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Phenol, 3-[(dimethylamino)methyl]-4-methyl-, acetate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102101-54-2

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102101-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102101-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102101-54:
(8*1)+(7*0)+(6*2)+(5*1)+(4*0)+(3*1)+(2*5)+(1*4)=42
42 % 10 = 2
So 102101-54-2 is a valid CAS Registry Number.

102101-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetic acid 3-dimethylaminomethyl-4-methyl-phenyl ester

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:102101-54-2 SDS

102101-54-2Downstream Products

102101-54-2Relevant academic research and scientific papers

Intermediate in Sommelet-Hauser Rearrangement of N,N-Dimethylbenzylammonium N-Methylides

Shirai, Naohiro,Watanabe, Yoko,Sato, Yoshiro

, p. 2767 - 2770 (2007/10/02)

Formation of benzylammonium N-methylides by fluoride anion induced desilylation of dimethyl(4-substituted benzyl)ammonium halides (1) and 3-substituted benzyl analogues (6) was examined to isolate 5--6-methylene-1,3-cyclohexadienes (isotoluene intermediates, 3,8,10) in the Sommelet-Hauser rearrangement.Some isotoluenes were isolated and their structures were confirmed by 1H NMR analysis.The stability of the isotoluenes was dependent on the electron-donating effects of the substituents on the conjugated bonds, and 3-methoxy-substituted isotoluene 3a was the most stable compound studied.

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