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Chloromethyl 2 Ethoxy 2 Methylpropanoate 1000296 74 1 Structure

Chloromethyl 2-ethoxy-2-methylpropanoate

Chloromethyl 2-ethoxy-2-methylpropanoate, identified by CAS number 1000296-74-1, is a specialized organic intermediate primarily utilized in the pharmaceutical and fine chemical industries. This compound features a chloromethyl ester functional group attached to a branched ethoxy-substituted propanoate backbone. Its unique structural configuration makes it a valuable reagent for the synthesis of complex molecules, particularly where the introduction

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Cefpirome Sulfate 98753 19 6 Structure

Cefpirome sulfate

Cefpirome sulfate (CAS 98753-19-6) is a sophisticated fourth-generation cephalosporin derivative utilized primarily as a high-purity chemical intermediate and reference standard in pharmaceutical research. Chemically, it is characterized by its zwitterionic structure, featuring a quaternary ammonium group at the C-3 position of the cephem nucleus, which enhances its penetration through the outer membrane of Gram-negative organisms.

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3 Ethoxy 4 Ethoxycarbonylphenylacetic Acid 99469 99 5 Structure

[3-Ethoxy-4-(ethoxycarbonyl)phenyl]acetic acid

[3-Ethoxy-4-(ethoxycarbonyl)phenyl]acetic acid, identified by CAS number 99469-99-5, is a high-purity organic building block characterized by its substituted aromatic framework. This compound features a phenylacetic acid core with an ethoxy group at the meta-position and an ethoxycarbonyl group at the para-position relative to the acetic acid side chain. As a white to off-white crystalline solid, it

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1 4 Aminophenoxy 3 Ethoxypropan 2 Ol 94056 98 1 Structure

1-(4-Aminophenoxy)-3-ethoxypropan-2-ol

1-(4-Aminophenoxy)-3-ethoxypropan-2-ol, identified by CAS number 94056-98-1, is a versatile organic building block characterized by its multi-functional molecular structure. It features a primary aromatic amine group attached to a phenoxy backbone, which is further substituted with a 3-ethoxypropan-2-ol side chain. This combination of functional groups—specifically the amine, ether, and secondary hydroxyl moieties—renders the compound highly reactive

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11 Dimethoxy 2 2 Methoxyethoxyethane 94158 44 8 Structure

1,1-Dimethoxy-2-(2-methoxyethoxy)ethane

1,1-Dimethoxy-2-(2-methoxyethoxy)ethane, identified by CAS 94158-44-8, is a specialized organic building block primarily utilized as a protected aldehyde intermediate in fine chemical synthesis. Structurally, the compound features a dimethyl acetal group and a methoxyethoxy ether chain, a combination that provides unique chemical stability and solubility characteristics. As an acetal, it remains stable under neutral and basic

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Methoxyethoxyundecyltrichlorosilane 943349 49 3 Structure 1024x768

Methoxyethoxyundecyltrichlorosilane

Methoxyethoxyundecyltrichlorosilane (CAS 943349-49-3) is a specialized organosilicon compound utilized primarily as a surface modification agent and molecular linker in advanced material science. Characterized by a long eleven-carbon undecyl spacer chain, it features a terminal trichlorosilyl group and a methoxyethoxy moiety. The trichlorosilyl functionality is highly reactive toward hydroxylated surfaces, such as glass, silicon dioxide, and

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Polysorbate 40 9005 66 7 Structure

Polysorbate 40

Polysorbate 40, identified by CAS number 9005-66-7, is a non-ionic surfactant and emulsifier derived from ethoxylated sorbitan esterified with palmitic acid. Chemically known as polyoxyethylene (20) sorbitan monopalmitate, it typically presents as a viscous, amber-colored liquid at room temperature. This material is characterized by its high hydrophilic-lipophilic balance (HLB) value, making it particularly effective at

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3 Triethoxysilylpropylsuccinic Anhydride 93642 68 3 Structure

3-(Triethoxysilyl)propylsuccinic anhydride

3-(Triethoxysilyl)propylsuccinic anhydride, identified by CAS 93642-68-3, is a bifunctional organosilane characterized by its reactive succinic anhydride group and hydrolyzable triethoxysilyl moiety. This chemical serves as a versatile bridge between inorganic substrates and organic polymer matrices. The triethoxysilyl group facilitates covalent bonding to hydroxyl-rich surfaces such as silica, glass, and metal oxides through silanol formation and

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Ethyl Ethoxymethylenecyanoacetate 94 05 3 Structure

Ethyl (ethoxymethylene)cyanoacetate

Ethyl (ethoxymethylene)cyanoacetate, identified by CAS number 94-05-3, is a highly functionalized organic compound that serves as a pivotal building block in fine chemical synthesis. Structurally, it features a cyano group and an ethyl ester group adjacent to an ethoxymethylene moiety, creating a versatile electrophilic center. This unique arrangement allows for a wide range of chemical

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E N 2 Chloro 6 Methylphenyl 3 Ethoxyacrylamide 863127 76 8 Structure

(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide

(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide, identified by CAS 863127-76-8, is a specialized organic building block primarily utilized in the pharmaceutical and fine chemical industries. Structurally, it is an alpha,beta-unsaturated amide derivative featuring a 2-chloro-6-methylphenyl substituent and a trans-configured ethoxy group. This compound serves as a pivotal intermediate in the multi-step synthesis of complex heterocyclic molecules, most notably tyrosine kinase

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S Ethyl 34 Dimethoxybicyclo420octa 135 Trien 7 Ylmethylcarbamate 869856 10 0 Structure

(S)-Ethyl ((3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl)methyl)carbamate

(S)-Ethyl ((3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl)methyl)carbamate, identified by CAS number 869856-10-0, is a specialized organic intermediate characterized by its rigid bicyclic benzocyclobutene framework and a carbamate functional group. This compound features two methoxy substituents on the aromatic ring and a chiral center at the 7-position, making it a valuable chiron in asymmetric synthesis. As a high-value chemical raw material,

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3R 1 3 Fluorophenyl 3 Pyrrolidinol 3 4 Methylbenzenesulfonate 873945 29 0 Structure

(3R)-1-(3-Fluorophenyl)-3-pyrrolidinol 3-(4-methylbenzenesulfonate)

(3R)-1-(3-Fluorophenyl)-3-pyrrolidinol 3-(4-methylbenzenesulfonate), identified by CAS number 873945-29-0, is a high-purity chiral building block utilized primarily in advanced organic synthesis. This compound features a pyrrolidine core substituted with a 3-fluorophenyl group at the nitrogen atom and a tosylate (4-methylbenzenesulfonate) ester at the 3-position. The (R)-enantiomeric configuration provides a defined stereochemical center, which is crucial for the

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Ethyl 4 2 13 Dioxo 13 Dihydro 2H Isoindol 2 Ylethoxy 3 Oxobutanoate 88150 75 8 Structure

Ethyl 4-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]-3-oxobutanoate

Ethyl 4-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]-3-oxobutanoate, identified by CAS number 88150-75-8, is a specialized organic intermediate widely utilized in the fine chemical and pharmaceutical industries. This compound is characterized by its complex structure, which incorporates a phthalimide-protected amino-ethoxy group attached to an ethyl acetoacetate derivative. As a functionalized beta-keto ester, it exhibits significant reactivity suitable for various condensation and

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4 Tert Butylphenyltetramethylenesulfonium Perfluoro 1 Butanesulfonate 900188 13 8 Structure

4-tert-Butylphenyltetramethylenesulfonium perfluoro-1-butanesulfonate

4-tert-Butylphenyltetramethylenesulfonium perfluoro-1-butanesulfonate, identified by CAS 900188-13-8, is a high-performance photoacid generator (PAG) belonging to the sulfonium salt family. This ionic compound features a bulky tert-butylphenyl substituted tetramethylenesulfonium cation paired with a nonafluorobutanesulfonate (nonaflate) anion. Its chemical architecture is specifically engineered to provide excellent thermal stability and high sensitivity to short-wavelength radiation, such as deep ultraviolet

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Bis4 Tert Butylphenyliodonium Triflate 84563 54 2 Structure

Bis(4-tert-butylphenyl)iodonium triflate

Bis(4-tert-butylphenyl)iodonium triflate, identified by CAS number 84563-54-2, is a high-performance diaryliodonium salt widely utilized as a photoacid generator (PAG) in advanced chemical processing. Characterized by its trifluoromethanesulfonate (triflate) anion and tert-butyl substituted phenyl groups, this compound exhibits excellent thermal stability and superior solubility in various organic monomers and solvent systems compared to unsubstituted analogs. In

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Di Tert Butylsilyl Bistrifluoromethanesulfonate 85272 31 7 Structure

Di-tert-butylsilyl bis(trifluoromethanesulfonate)

Di-tert-butylsilyl bis(trifluoromethanesulfonate), identified by CAS number 85272-31-7, is a highly reactive organosilicon reagent frequently employed in advanced organic synthesis and pharmaceutical research. Often referred to as di-tert-butylsilyl ditriflate, this compound features a silicon center bonded to two bulky tert-butyl groups and two trifluoromethanesulfonate (triflate) leaving groups. The presence of the triflate groups makes it an

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