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2-IMINO-3-METHYLCYCLOPENTANECARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

903631-60-7

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903631-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 903631-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,6,3 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 903631-60:
(8*9)+(7*0)+(6*3)+(5*6)+(4*3)+(3*1)+(2*6)+(1*0)=147
147 % 10 = 7
So 903631-60-7 is a valid CAS Registry Number.

903631-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-imino-3-methylcyclopentane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-IMINO-3-METHYLCYCLOPENTANECARBONITRILE

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:903631-60-7 SDS

903631-60-7Downstream Products

903631-60-7Relevant academic research and scientific papers

Syntheses and biological activities of octahydro-1H-cyclopenta[d]pyrimidine derivatives

Tian, Zhongzhen,Jiang, Zhaoxing,Li, Zhong,Song, Gonghua,Huang, Qingchun

, p. 143 - 147 (2007)

Various nitromethylene derivatives were synthesized regioselectively. Compounds 8a-f were obtained by the reaction of 1-((5-chloropyridin-2-yl)methyl) -2-(nitromethylene)-octahydro-1H-cyclopenta[d]-pyrimidine (3) with primary amines and formaldehyde. The synthesized compounds were identified by 1H NMR, HRMS (EI), and IR, and preliminary bioassays indicated that most of them showed moderate insecticidal activities against Aphis craccivora. The relationship between hydrophobicity and biological activity was also discussed.

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