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119991-79-6

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119991-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119991-79-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,9 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119991-79:
(8*1)+(7*1)+(6*9)+(5*9)+(4*9)+(3*1)+(2*7)+(1*9)=176
176 % 10 = 6
So 119991-79-6 is a valid CAS Registry Number.

119991-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(methoxymethyl)benzyl acetate

1.2 Other means of identification

Product number -
Other names Essigsaeure-(4-methoxymethyl-benzylester)

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:119991-79-6 SDS

119991-79-6Downstream Products

119991-79-6Relevant articles and documents

Oxidation of benzylic alcohols and ethers to carbonyl derivatives by nitric acid in dichloromethane

Strazzolini, Paolo,Runcio, Antonio

, p. 526 - 536 (2007/10/03)

Nitric acid in dichloromethane may be successfully employed for the oxidation of benzylic alcohols and ethers to the corresponding carbonyl compounds. The proposed method proved to be of general applicability, affording very good yields of aldehydes and ketones and showing interesting chemoselectivity in many instances, allowing competitive aromatic nitration to be avoided, as well as - in the case of aldehydes - any further oxidation to carboxylic acids. The reaction probably proceeds by a radical mechanism, the active species in the oxidation process being NO2. Competitive formation of nitro esters was observed in some cases, whereas poor results were obtained with allylic and non-benzylic substrates. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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