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6296-92-0

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6296-92-0 Usage

Functional groups

Two hydroxyl (-OH) groups

Type of compound

Diol

Natural occurrence

Found in certain plant oils

Industrial applications

Used in various industries

Physical state

Colorless, odorless liquid

Boiling point

Relatively high boiling point

Solvent properties

Useful as a solvent

Production

Component in the production of various chemicals and materials

Pharmaceutical use

Used in some pharmaceutical products

Synthesis

Precursor in the synthesis of other organic compounds

Versatility

Wide range of uses in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 6296-92-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6296-92:
(6*6)+(5*2)+(4*9)+(3*6)+(2*9)+(1*2)=120
120 % 10 = 0
So 6296-92-0 is a valid CAS Registry Number.

6296-92-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethylcyclopentane-1,2-diol

1.2 Other means of identification

Product number -
Other names trans-1.2-Dimethylcyclopentan-1.2-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6296-92-0 SDS

6296-92-0Downstream Products

6296-92-0Relevant articles and documents

Regioselective synthesis of α,α-dialkylcyclopentanones from 1-hydroxycyclobutanecarboxylic acid or from O-protected cyclobutanone cyanohydrin

Estieu, Karine,Ollivier, Jean,Salauen, Jacques

, p. 8075 - 8090 (2007/10/03)

1-(1-Hydroxyalkyl)cyclobutanols 4a-f, readily available either from 1-hydroxycyclobutane carboxylic acid or from O-protected cyclobutanone cyanohydrin, appeared the most suitable precursors for a regioselective synthesis of cyclopentanones α,α- disubstituted with various similar or different alkyl, alkenyl, aryl or cycloalkyl groups. The key steps consist of acid or Grignard reagent induced C4→C5 ring expansions.

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