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425206

Sigma-Aldrich

2-(Methylthio)cyclohexanone

98%

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About This Item

Linear Formula:
CH3SC6H9(=O)
CAS Number:
Molecular Weight:
144.23
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

form

liquid

refractive index

n20/D 1.508 (lit.)

bp

45 °C/10.1 mmHg (lit.)

density

1.069 g/mL at 25 °C (lit.)

SMILES string

CSC1CCCCC1=O

InChI

1S/C7H12OS/c1-9-7-5-3-2-4-6(7)8/h7H,2-5H2,1H3

InChI key

QFABNUVNDKOIEH-UHFFFAOYSA-N

General description

2-(Methylthio)cyclohexanone is a 2-substituted cyclohexanone. The proportion of axial and equatorial conformation has been measured in chloroform by the Eliel method. It suggests that the in chloroform steric effect dominates over polar effect in contributing to the conformational preference. The stereoselectivity of the reduction of 2-(methylthio)cyclohexanone using different hydrides has been studied.

Application

2-(Methylthio)cyclohexanone may be used as a ketone substrate for the synthesis of cyclic nitrones, by reacting with aspergillusol A.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

192.2 °F - closed cup

Flash Point(C)

89 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

425206-BULK:
425206-VAR:
425206-1G:
425206-5G:


Certificates of Analysis (COA)

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Axial/equatorial proportions for 2-substituted cyclohexanones.
Basso EA, et al.
The Journal of Organic Chemistry, 58(27), 7865-7869 (1993)
Studies on the stereoselectivity of hydride reductions on 2-(methylthio)-and 2-(methylsulfonyl) cyclohexanones.
Carmen CM, et al.
The Journal of Organic Chemistry, 52(16), 3619-3625 (1987)
Nitrone formation in phosphate buffer and aqueous solutions: novel chemistry inspired by a natural product.
Pansanit A, et al.
Tetrahedron Letters, 53(16), 2129-2131 (2012)

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