(1S,2S)-Methoxycyclohexanol

CAS Number: 134108-92-2

Molecular Formula: C7H14O2

About (1S,2S)-Methoxycyclohexanol

(1S,2S)-2-Methoxycyclohexanol CAS 134108-92-2 serves as a vital chiral building block in the API intermediates market, where its precise stereochemistry is leveraged via custom synthesis services to develop enantiomerically pure anticonvulsants and antidepressants with 99% pharma-grade purity. (1S,2S)-(+)-2-Methoxycycl...

(1S,2S)-Methoxycyclohexanol Specifications

CAS Number

134108-92-2

Molecular Formula

C7H14O2

Molecular Weight

130.18 g/mol

IUPAC Name

trans-(1S,2S)-2-methoxycyclohexan-1-ol

Canonical SMILES

CO[C@H]1CCCC[C@@H]1O

InChI Key

DCQQZLGQRIVCNH-BQBZGAKWSA-N

CAS Number

134108-92-2

Molecular Formula

C7H14O2

Molecular Weight

130.18 g/mol

IUPAC Name

trans-(1S,2S)-2-methoxycyclohexan-1-ol

Canonical SMILES

CO[C@H]1CCCC[C@@H]1O

InChI Key

DCQQZLGQRIVCNH-BQBZGAKWSA-N

Molecular Weight

130.18 g/mol

Pharmaceutical Intermediate

A key chiral building block utilized in the synthesis of tricyclic beta-lactam antibiotics and other complex medicinal compounds

Agrochemical Intermediate

A versatile chiral starting material employed in the production of enantiomerically pure pesticides and herbicides to improve effectiveness and selectivity

Organic Synthesis Building Block

A functionalized cyclohexane derivative used as a chiral auxiliary or intermediate in the development of fine chemicals with precise stereochemistry

Fragrance and Flavor Ingredient

A specialty chemical component used in the formulation of perfumes and cosmetic products due to its unique scent profile

Research Tool

A chemical reagent used in academic and industrial studies to investigate stereoselective synthesis, chelation-controlled reductions, and the behavior of chiral molecules.