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1017781-46-2

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1017781-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1017781-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,7,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1017781-46:
(9*1)+(8*0)+(7*1)+(6*7)+(5*7)+(4*8)+(3*1)+(2*4)+(1*6)=142
142 % 10 = 2
So 1017781-46-2 is a valid CAS Registry Number.

1017781-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[2-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names Ethyl 3-(2-((tert-butoxycarbonyl)amino)phenyl)-3-oxopropanoate

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:1017781-46-2 SDS

1017781-46-2Relevant articles and documents

Intermediate compound for synthesizing nitrogen-containing heterocyclic ring and preparation method and application thereof

-

, (2021/04/21)

The invention relates to an intermediate compound for synthesizing a nitrogen-containing heterocyclic ring and a preparation method and application thereof, and the chemical structural formula of the intermediate compound is as follows: amide, azodicarboxylate and carboxylic acid are used as raw materials, and under the action of a catalyst, the intermediate compound is prepared through direct carbon-hydrogen bond bifunctionalization synthesis. Compared with the prior art, the method has the advantages that the intermediate compound is synthesized through the direct carbon-hydrogen bond bifunctionalization process, the substrate can be expanded in a large range, different nitrogen-containing heterocycles can be obtained through different subsequent treatment, the structural diversity is achieved, and a new method is provided for industrial production of the nitrogen-containing heterocycles.

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