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2313-61-3

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2313-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2313-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2313-61:
(6*2)+(5*3)+(4*1)+(3*3)+(2*6)+(1*1)=53
53 % 10 = 3
So 2313-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-4-6(2)5-7(3)8/h6-8H,4-5H2,1-3H3

2313-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHYL-2-HEXANOL

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-1-pentanol

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:2313-61-3 SDS

2313-61-3Relevant articles and documents

Alkane oxygenation catalysed by gold complexes

Shul'Pin, Georgiy B.,Shilov, Alexander E.,Süss-Fink, Georg

, p. 7253 - 7256 (2007/10/03)

Gold(III) and gold(I) complexes, NaAuCl4 and ClAuPPh3, efficiently catalyse the oxidation of alkanes by H2O2 in acetonitrile solution at 75°C. Turnover numbers (TONs) attain 520 after 144 h. Alkyl hydroperoxides are the main products, whereas ketones (aldehydes) and alcohols are formed in smaller concentrations. It is suggested on the basis of the bond selectivity study that at least one of the pathways in Au-catalysed alkane hydroperoxidation does not involve the participation of free hydroxyl radicals. Possibly, the oxidation begins from the alkane hydrogen atom abstraction by a gold oxo species. The oxidation of cyclooctane by air at room temperature catalysed by NaAuCl4 in the presence of Zn/CH3COOH as a reducing agent and methylviologen as an electron-transfer agent gave cyclooctanol (TON=10).

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