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3938-10-1

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3938-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3938-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3938-10:
(6*3)+(5*9)+(4*3)+(3*8)+(2*1)+(1*0)=101
101 % 10 = 1
So 3938-10-1 is a valid CAS Registry Number.

3938-10-1SDS

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 3,4,5-trimethylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 1,2-Benzenediol,3,4,5-trimethyl

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:3938-10-1 SDS

3938-10-1Downstream Products

3938-10-1Relevant articles and documents

Efficient ortho-oxidation of phenols with diacyl peroxides

Tada, Masahiro,Ishiguro, Risa,Izumi, Ryohei

, p. 239 - 242 (2008/09/21)

A stable symmetric diacyl peroxide, m-chlorobenzoyl peroxide (mCBPO), and an asymmetric diacyl peroxide, chloroacetyl m-chlorobenzoyl peroxide (CAMCBPO), were synthesized from m-chloroperbenzoic acid. Both peroxides oxidized phenols selectively at the ortho position predoninantly. CAMCBPO gave para-oxidized compounds as minor products from some phenols. The improvement of the yield of ortho-oxidation of phenols with mCBPO was also reported.

Trimethylcatechol diester and a method for producing the same

-

, (2008/06/13)

This method provides a novel trimethylcatechol diester, i.e. 3,4,5-trimethylcatechol diester, at a high yield by reacting 2,6,6-trimethylcyclohexe-2-en-1,4-dione with an acylating agent in the presence of an acid catalyst. The acylating agent includes a C2-4 carboxylic acid anhydride (e.g. acetic anhydride) and a C2-4 carboxylic acid halide (e.g. acetyl chloride). The catalyst includes a protonic acid and a Lewis acid. Use of a polar solvent (e.g. halogenated hydrocarbon), as the reaction catalyst, results in an enhanced efficiency in the production of the object compound.

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