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4 Vinylguaiacol 7786 61 0 Structure

4-Vinylguaiacol

4-Vinylguaiacol, identified by CAS number 7786-61-0, is a naturally occurring phenolic compound renowned for its distinct aromatic profile. Chemically known as 2-methoxy-4-vinylphenol, it presents as a colorless to pale yellow liquid or crystalline solid depending on ambient temperature. It is a key volatile component found in various fermented and roasted products, such as roasted coffee,

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Musk Ambrette 83 66 9 Structure

4-tert-Butyl-2,6-dinitro-3-methoxytoluene

Musk ambrette, identified by CAS number 83-66-9, is a prominent synthetic nitro-musk compound recognized for its intense and persistent fragrance profile. It typically appears as pale yellow crystals or a crystalline powder, exhibiting a characteristic musk odor with distinct floral and ambrette-seed-like undertones. Chemically known as 2,6-dinitro-3-methoxy-4-tert-butyltoluene, this compound is prized for its excellent fixative

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4 Methoxycinnamic Acid 830 09 1 Structure

4-Methoxycinnamic acid

4-Methoxycinnamic acid, identified by CAS number 830-09-1, is a substituted cinnamic acid derivative characterized by a methoxy group at the para position of the benzene ring. It typically appears as a white to pale yellow crystalline powder. As an organic compound, it serves as a foundational building block in various chemical syntheses due to its

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2 Propene 1 Thiol 870 23 5 Structure

2-Propene-1-thiol

2-Propene-1-thiol, commonly referred to as allyl mercaptan, is an organosulfur compound characterized by its distinct, pungent odor reminiscent of garlic and onions. Identified by CAS number 870-23-5, this clear to pale yellow liquid is a highly reactive thiol featuring a terminal alkene group. Its dual functionality makes it a versatile building block in organic chemistry,

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Benzyl Methyl Sulfide 766 92 7 Structure

Benzyl methyl sulfide

Benzyl methyl sulfide, identified by CAS number 766-92-7, is an organosulfur compound characterized by a thioether linkage connecting a methyl group and a benzyl group. It typically appears as a clear to pale yellow liquid with a distinct, pungent odor characteristic of sulfides. As a stable thioether, it serves as a versatile building block in

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Benzyl Methyl Disulfide 699 10 5 Structure

Benzyl methyl disulfide

Benzyl methyl disulfide, identified by CAS number 699-10-5, is a specialized organosulfur compound characterized by its distinct unsymmetrical disulfide bridge connecting a benzyl group and a methyl group. This clear to pale yellow liquid is recognized for its potent and characteristic sulfurous aroma, which is often associated with natural volatile components found in Allium species

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1 P Menthene 8 Thiol 71159 90 5 Structure

1-p-Menthene-8-thiol

1-p-Menthene-8-thiol, commonly known as grapefruit mercaptan, is a highly potent organosulfur compound with the CAS registry number 71159-90-5. Structurally related to limonene, this terpene thiol is recognized as one of the most powerful aroma chemicals in existence, possessing an incredibly low odor detection threshold. In its concentrated form, the substance exhibits a sharp, sulfurous profile,

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Pyrazine 2 Ethoxy 3 1 Methylethyl 72797 16 1 Structure

Pyrazine, 2-ethoxy-3-(1-methylethyl)-

Pyrazine, 2-ethoxy-3-(1-methylethyl)-, also known as 2-ethoxy-3-isopropylpyrazine, is a specialized heterocyclic aromatic compound belonging to the pyrazine family. This chemical is distinguished by the presence of both an ethoxy group and an isopropyl substituent on the pyrazine ring, a configuration that imparts significant organoleptic potency. In its physical form, it is typically a colorless to pale

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2 Methyl 3 Propyldisulfanyl Furan 61197 09 9 Structure

2-methyl-3-(propyldisulfanyl)furan

2-methyl-3-(propyldisulfanyl)furan, identified by CAS 61197-09-9, is a specialized organosulfur compound characterized by a furan ring substituted with a propyldisulfanyl group. This colorless to pale yellow liquid is highly valued in the chemical and flavor industries for its potent and distinctive organoleptic properties. As a member of the furanoid disulfide family, it exhibits a complex aromatic

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Furfuryl Acetate 623 17 6 Structure

Furfuryl acetate

Furfuryl acetate, identified by CAS number 623-17-6, is an organic ester compound characterized by its distinct aromatic profile. It typically appears as a colorless to pale yellow liquid and is derived from the esterification of furfuryl alcohol with acetic acid. This chemical is known for its spicy, floral, and slightly fruity scent, which makes it

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Furfuryl Propionate 623 19 8 Structure

Furfuryl propionate

Furfuryl propionate, identified by CAS number 623-19-8, is a clear to pale yellow liquid ester derived from the reaction between furfuryl alcohol and propionic acid. This organic compound belongs to the furan family and is characterized by its distinctively warm, spicy, and woody aroma, often accompanied by subtle fruity undertones. Its chemical structure features a

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2 5 Dimethyl 4 Ethoxy 3 2H Furanone 65330 49 6 Structure

2,5-Dimethyl-4-ethoxy-3(2H)-furanone

2,5-Dimethyl-4-ethoxy-3(2H)-furanone, identified by CAS number 65330-49-6, is a specialized heterocyclic organic compound belonging to the furanone family. It is recognized for its distinctive organoleptic profile, characterized by a potent, sweet, and fruity aroma reminiscent of cooked sugar and berries. This compound is a derivative of the naturally occurring flavor compound Furaneol, where the ethoxy substitution

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DL 10 Camphorsulfonic Acid 5872 08 2 Structure

DL-10-Camphorsulfonic acid

DL-10-Camphorsulfonic acid, identified by CAS 5872-08-2, is a robust organosulfur compound characterized as a racemic mixture of camphorsulfonic acid enantiomers. It typically appears as a white to off-white crystalline solid and is highly valued for its strong acidic properties combined with a bulky, lipophilic camphor skeleton. This unique structure allows it to function effectively in

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2 Mercaptomethyl Pyrazine 59021 02 2 Structure

2-mercaptomethyl pyrazine

2-Mercaptomethyl pyrazine, identified by CAS number 59021-02-2, is a specialized organosulfur compound characterized by a pyrazine ring substituted with a mercaptomethyl group. This heterocyclic molecule is recognized for its potent and distinctive organoleptic properties, exhibiting a powerful aroma that combines sulfurous, roasted, and savory notes. In its pure form, it typically appears as a clear

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2 5 Dimethylfuran 3 Thiol 55764 23 3 Structure

2,5-Dimethylfuran-3-thiol

2,5-Dimethylfuran-3-thiol, identified by CAS number 55764-23-3, is a specialized organosulfur compound characterized by its distinct furan ring substituted with two methyl groups and a thiol functional group. This colorless to pale yellow liquid is recognized for its potent and complex aromatic profile, which is highly valued in chemical synthesis and sensory applications. As a member

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