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803683-16-1

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803683-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 803683-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,3,6,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 803683-16:
(8*8)+(7*0)+(6*3)+(5*6)+(4*8)+(3*3)+(2*1)+(1*6)=161
161 % 10 = 1
So 803683-16-1 is a valid CAS Registry Number.

803683-16-1SDS

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 2-[(2-methyl-1-methylsulfanylpropan-2-yl)carbamoyl]benzoic acid

1.2 Other means of identification

Product number -
Other names N-[1,1-dimethyl-2-(methylthio)ethyl]phthalamic acid

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:803683-16-1 SDS

803683-16-1Downstream Products

803683-16-1Relevant articles and documents

PROCESS FOR PRODUCING 2-HALOGENOBENZAMIDE COMPOUND

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Page/Page column 15, (2008/06/13)

A novel process for producing a 2-halogenobenzamide compound useful as a raw material or active ingredient for medicines and agricultural chemicals. The process, which is for producing a 2-halogenobenzamide compound represented by the general formula (I): (wherein R1, R2, R3, R4, and R6 may be the same or different and each represents hydrogen or C1-6 alkyl; R5 represents C1-6 alkyl; k is 1 or 2; Y1, Y2, Y3, and Y4 may be the same or different and each represents hydrogen, halogeno, etc.; and X represents chlorine, bromine, or iodine), is characterized by reacting an benzamide compound with a halogenating agent in the presence of a palladium catalyst to obtain a substituted benzamide compound and then reacting the resultant substituted benzamide compound with an oxidizing agent after or without isolating the substituted benzamide compound.

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