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I Pinene 7785 26 4 Structure

I+–Pinene, (-)-

(-)-alpha-Pinene, identified by CAS 7785-26-4, is a naturally occurring bicyclic monoterpene and a primary constituent of various essential oils, most notably those derived from coniferous trees. As a clear, colorless liquid with a distinctively woody and pine-like aroma, it serves as a fundamental building block in the terpene chemistry landscape. This isomer is characterized by

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3 3 4 Dimethoxyphenyl 2 Propenenitrile 6443 72 7 Structure

3-(3,4-Dimethoxyphenyl)-2-propenenitrile

3-(3,4-Dimethoxyphenyl)-2-propenenitrile, identified by CAS number 6443-72-7, is a specialized organic compound characterized by its substituted cinnamonitrile structure. It features a propenenitrile backbone linked to a benzene ring with two methoxy groups at the 3 and 4 positions. This chemical is typically encountered as a crystalline solid and serves as a versatile building block in the

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2 3H Furanone 5 Ethyldihydro 695 06 7 Structure

2(3H)-Furanone, 5-ethyldihydro-

2(3H)-Furanone, 5-ethyldihydro-, commonly known as gamma-caprolactone, is a versatile cyclic ester characterized by its distinct organoleptic properties. Identified by the CAS number 695-06-7, this compound typically appears as a colorless to slightly yellowish liquid at room temperature. It is recognized for its relative stability under standard conditions, although it should be handled with the standard

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5 Hydroxyoctanoic Acid Lactone 698 76 0 Structure

5-Hydroxyoctanoic acid lactone

5-Hydroxyoctanoic acid lactone, widely recognized in the chemical industry as delta-octalactone, is a cyclic ester belonging to the delta-lactone family. Identified by CAS number 698-76-0, this organic compound is characterized by its distinct six-membered ring structure. It typically presents as a clear to slightly yellowish liquid with a high boiling point. Its chemical stability and

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2 3H Furanone 5 Hexyldihydro 706 14 9 Structure

2(3H)-Furanone, 5-hexyldihydro-

2(3H)-Furanone, 5-hexyldihydro-, widely recognized in the specialty chemical industry as gamma-decalactone, is a naturally occurring lactone that serves as a fundamental building block in the flavor and fragrance sectors. This compound is characterized by its distinct, intense aroma reminiscent of ripe peaches and apricots, presenting as a clear to pale yellow oily liquid. As a

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L Borneol 464 45 9 Structure

L-Borneol

L-Borneol, identified by CAS number 464-45-9, is a naturally occurring bicyclic monoterpene alcohol characterized by its distinct, pungent, and slightly camphoraceous aroma. As a specific isomer of borneol, the L-form exhibits characteristic optical activity and typically appears as a white to off-white crystalline solid or translucent mass. It is highly valued across various industrial sectors

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4 Aminocinnamic Acid Ethyl Ester 5048 82 8 Structure

4-aminocinnamic acid ethyl ester

4-Aminocinnamic acid ethyl ester, identified by CAS number 5048-82-8, is a versatile organic compound belonging to the cinnamate ester family. Characterized by the presence of both an amino group and an alpha, beta-unsaturated ester moiety, this molecule serves as a significant building block in synthetic organic chemistry. It typically appears as a pale yellow to

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3 1 1 Biphenyl 3 Yl Acrylic Acid 60521 26 8 Structure

3-([1,1′-Biphenyl]-3-yl)acrylic acid

3-([1,1′-Biphenyl]-3-yl)acrylic acid, identified by CAS number 60521-26-8, is a specialized organic compound characterized by a biphenyl moiety substituted with a propenoic acid group at the meta-position. This structural configuration provides a rigid, conjugated backbone that is highly valued in synthetic chemistry. The compound typically appears as a crystalline solid and exhibits chemical properties consistent with

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4 Dimethylamino Cinnamaldehyde 6203 18 5 Structure

4-(Dimethylamino)cinnamaldehyde

4-(Dimethylamino)cinnamaldehyde, identified by CAS number 6203-18-5, is an aromatic organic compound characterized by its distinct cinnamaldehyde backbone substituted with a dimethylamino group at the para position. This chemical typically appears as a yellow to orange-brown crystalline solid or powder. It is recognized for its reactivity as an electrophile and its ability to undergo condensation reactions

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Hexyl Salicylate 6259 76 3 Structure

Hexyl salicylate

Hexyl salicylate, identified by CAS number 6259-76-3, is a clear, colorless to pale yellow liquid ester widely recognized for its mild, sweet, and floral-balsamic aroma. As a derivative of salicylic acid, it exhibits excellent stability and low volatility, making it a reliable component in various chemical formulations. Its chemical structure provides a smooth, tenacious scent

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5 Hydroxynonanoic Acid Lactone 3301 94 8 Structure

5-Hydroxynonanoic acid, lactone

5-Hydroxynonanoic acid, lactone, identified by the CAS number 3301-94-8 and commonly known as delta-nonalactone, is a cyclic ester that serves as a vital component in the flavor and fragrance industries. This organic compound is characterized by its distinct creamy, milky, and coconut-like aroma, which provides a rich sensory profile to various formulations. Physically, it typically

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Ethyl 2 Methylpentanoate 39255 32 8 Structure

Ethyl 2-methylpentanoate

Ethyl 2-methylpentanoate, identified by CAS number 39255-32-8, is a versatile organic ester widely recognized for its distinctive and potent olfactory profile. Characterized as a clear, colorless liquid, this compound exhibits a low viscosity and a high degree of solubility in organic solvents. Its chemical structure, featuring a branched pentanoate chain, contributes to its unique sensory

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3 Bromo 1 1 4 Trichloro 1 Fluorobutane 406 67 7 Structure

3-Bromo-1,1,4-Trichloro-1-Fluorobutane

3-Bromo-1,1,4-trichloro-1-fluorobutane, identified by CAS number 406-67-7, is a specialized halogenated organic compound characterized by its unique substitution pattern of bromine, chlorine, and fluorine atoms on a butane backbone. As a multi-halogenated alkane, it serves as a versatile building block in complex organic synthesis, particularly where selective functionalization is required. The presence of multiple halogen groups

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3 4 Fluorophenyl 2 Propenoic Acid 459 32 5 Structure

3-(4-fluorophenyl)-2-propenoic acid

3-(4-fluorophenyl)-2-propenoic acid, also widely recognized as 4-fluorocinnamic acid, is an organic compound characterized by its cinnamic acid backbone with a fluorine substituent at the para position of the benzene ring. This white to off-white crystalline solid serves as a versatile building block in synthetic chemistry, owing to the presence of both an alpha, beta-unsaturated carboxylic

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