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100377-16-0

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100377-16-0 Usage

Uses

n-(2-cyano-cyclopent-1-enyl)-acetamide is a useful chemical for the hydrogenation of β-?acetylaminoacrylonitriles.

Check Digit Verification of cas no

The CAS Registry Mumber 100377-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,7 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100377-16:
(8*1)+(7*0)+(6*0)+(5*3)+(4*7)+(3*7)+(2*1)+(1*6)=80
80 % 10 = 0
So 100377-16-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O/c1-6(11)10-8-4-2-3-7(8)5-9/h2-4H2,1H3,(H,10,11)

100377-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-cyanocyclopenten-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names N-(2-cyanocyclopent-1-en-1-yl)acetamide

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:100377-16-0 SDS

100377-16-0Downstream Products

100377-16-0Relevant articles and documents

Copper-catalyzed oxidative ring closure of ortho-cyanoanilides with hypervalent iodonium salts: Arylation-ring closure approach to iminobenzoxazines

Aradi, Klra,Novk, Zoltn

, p. 371 - 376 (2015)

A novel, highly modular synthetic methodology with high functional group tolerance was developed for the construction of iminobenzoxazine derivatives from ortho-cyanoanilides and diaryliodonium triflates via an oxidative arylation-cyclization path. The reaction is supposed to involve the formation of highly active aryl-copper(III) species. In this novel transformation, copper(II) triflate was used as catalyst in 1,2-dichloroethane or ethyl acetate and the reaction takes place at 75 °C in 2-16 h.

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