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106107-52-2

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106107-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106107-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106107-52:
(8*1)+(7*0)+(6*6)+(5*1)+(4*0)+(3*7)+(2*5)+(1*2)=82
82 % 10 = 2
So 106107-52-2 is a valid CAS Registry Number.

106107-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4-dimethoxy-phenyl)-carbamic acid methyl ester

1.2 Other means of identification

Product number -
Other names (3,4-Dimethoxy-phenyl)-carbamidsaeure-methylester

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:106107-52-2 SDS

106107-52-2Relevant articles and documents

An efficient modification of the Hofmann rearrangement: synthesis of methyl carbamates

Gogoi, Pranjal,Konwar, Dilip

, p. 531 - 533 (2007)

A series of methyl carbamates was synthesized using NaOCl as an oxidant in the presence of KF/Al2O3/MeOH at reflux in excellent yields.

Aerobic oxidative homocoupling reaction of anilides using heterogeneous metal catalysts

Fujimoto, Shigenobu,Matsumoto, Kenji,Iwata, Takayuki,Shindo, Mitsuru

supporting information, p. 973 - 976 (2017/02/15)

We have developed a heterogeneous catalytic oxidative homocoupling reaction of dimethoxyanilides under an oxygen atmosphere. The resulting homo-dimers are useful for the construction of heterocycles, demonstrating the potential of heterogeneous metal catalysts.

Alkyl 2-carboalkoxy-3,4-dialkoxybenzenecarbamates and process for their preparation

-

, (2008/06/13)

A process for the preparation of alkyl 2-carboxy-3,4-dialkoxybenzenecarbamates is described. The carbamates are useful intermediates in the preparation of 8-halo-5,6-dialkoxyquinazoline-2,4-diones. The diones are useful as cardiotonic agents.

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