CAS 149488-89-1

2-cyclohex-1-enylethyl isothiocyanate

Description:

2-Cyclohex-1-enylethyl isothiocyanate is an organic compound characterized by the presence of an isothiocyanate functional group (-N=C=S) attached to a cyclohexene moiety. This compound features a cyclohexene ring, which contributes to its cyclic structure and potential reactivity. Isothiocyanates are known for their pungent odor and are often associated with various biological activities, including antimicrobial and anticancer properties. The presence of the cyclohexene ring may influence the compound's reactivity and stability, as well as its interactions with biological systems. Additionally, isothiocyanates are typically formed from the hydrolysis of glucosinolates, which are found in cruciferous vegetables. The compound's molecular structure suggests it may participate in nucleophilic reactions, making it of interest in synthetic organic chemistry. Overall, 2-cyclohex-1-enylethyl isothiocyanate represents a unique chemical entity with potential applications in pharmaceuticals and agrochemicals, warranting further investigation into its properties and effects.

Formula: C₉H₁₃NS

InChI: InChI=1/C9H13NS/c11-8-10-7-6-9-4-2-1-3-5-9/h4H,1-3,5-7H2

SMILES: C1CC=C(CC1)CCN=C=S

Synonyms:

• 1-(2-Isothiocyanatoethyl)Cyclohexene

Cyclohexene, 1-(2-isothiocyanatoethyl)-

CAS: 149488-89-1

Formula: C₉H₁₃NS

Molecular weight: 167.2712

Ref: IN-DA001LQY

1-[2-(Isothiocyanato)ethyl]cyclohex-1-ene

CAS: 149488-89-1

1-[2-(Isothiocyanato)ethyl]cyclohex-1-ene

Purity: 95%

Molecular weight: 167.27g/mol

Ref: 54-OR3001