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67698-75-3

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67698-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67698-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,9 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67698-75:
(7*6)+(6*7)+(5*6)+(4*9)+(3*8)+(2*7)+(1*5)=193
193 % 10 = 3
So 67698-75-3 is a valid CAS Registry Number.

67698-75-3SDS

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 2,5-dimethoxybenzyl acetate

1.2 Other means of identification

Product number -
Other names -

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:67698-75-3 SDS

67698-75-3Relevant articles and documents

Environmentally benign decarboxylative: N-, O-, and S-Acetylations and acylations

Ghosh, Santanu,Purkait, Anisha,Jana, Chandan K.

supporting information, p. 8721 - 8727 (2020/12/30)

An operationally simple and general method for acetylation and acylation of a wide variety of substrates (amines, alcohols, phenols, thiols, and hydrazones) has been reported. Meldrum's acid and its derivatives have been used as an air-stable, non-volatile, cost-effective, and easy to handle acetylating/acylating agent. Easily separable byproducts (CO2 and acetone) allowed the isolation of analytically pure acetylated products without the requirement of work-up and any chromatography. This journal is

A facile one-step conversion of aromatic aldehydes to acetates

Baruah

, p. 60 - 61 (2007/10/03)

Aromatic aldehydes are efficiently converted to the corresponding benzyl acetates with acetic anhydride and zinc in the presence of acidic aluminium oxide in dichloromethane at room temperature.

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