Menthyl Chloride

CAS Number: 16052-42-9

Molecular Formula: C10H19Cl

About Menthyl Chloride

Menthyl chloride (CAS No: 16052-42-9) serves as a critical chiral building block in the global speciality chemical market, particularly valued in asymmetric synthesis for its ability to impart specific stereochemical outcomes in the construction of complex bioactive molecules. In the flavour and fragrance sector, this ...

Menthyl Chloride Specifications

CAS Number

16052-42-9

Molecular Formula

C10H19Cl

Molecular Weight

174.71

IUPAC Name

(1S,2R,4R)-2-chloro-4-methyl-1-propan-2-ylcyclohexane

Canonical SMILES

ClC1CC(C)CCC1C(C)C

InChI Key

OMLOJNNKKPNVKN-KXUCPTDWSA-N

HSN No

29038930

CAS Number

16052-42-9

Molecular Formula

C10H19Cl

Molecular Weight

174.71

IUPAC Name

(1S,2R,4R)-2-chloro-4-methyl-1-propan-2-ylcyclohexane

Canonical SMILES

ClC1CC(C)CCC1C(C)C

InChI Key

OMLOJNNKKPNVKN-KXUCPTDWSA-N

HSN No

29038930

Molecular Weight

174.71

Melting Point (Experimental)

-20.1-16.5 °C

Boiling Point (Experimental)

90-95°C Press: 170 Torr

Density (Experimental)

0.936 g/cm³ Temp: 420 °C

Flavor and Fragrance Industry

A versatile organic compound commonly used as a flavoring agent in food products and a fragrance component in cosmetics to provide a refreshing minty scent and cooling sensation

Organic Synthesis Building Block

A chiral halogenated intermediate utilized in academic and industrial research for the synthesis of menthol derivatives, complex organic molecules, and asymmetric hydrogenation catalyst ligands

Pharmaceutical Intermediate

A critical chemical building block employed in the preparation of medicinal compounds, including those for respiratory ailments and pharmaceutical precursors such as phenol ethers

Chemical Reagent

An electrophilic cyclohexane derivative used in specialized chemical reactions, such as E2 eliminations and nucleophilic substitutions, to develop molecules with specific stereochemistry