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55817-74-8

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55817-74-8 Usage

Structure

Consists of a pyrrole ring with a cyclohexyl and two methyl groups attached

Functional Groups

Carbonitrile (–C≡N): Indicates the presence of a nitrile functional group
Amino (–NH2): Suggests the presence of a basic nitrogen atom

Potential Applications

Pharmaceuticals
Organic synthesis
Materials science

Unique Properties

Complex structure with diverse functional groups
Potential for various chemical reactions
Valuable compound for research and development in chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 55817-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,1 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55817-74:
(7*5)+(6*5)+(5*8)+(4*1)+(3*7)+(2*7)+(1*4)=148
148 % 10 = 8
So 55817-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H19N3/c1-9-10(2)16(13(15)12(9)8-14)11-6-4-3-5-7-11/h11H,3-7,15H2,1-2H3

55817-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-cyclohexyl-4,5-dimethylpyrrole-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Amino-1-cyclohexyl-4,5-dimethyl-3-pyrrolcarbonitril

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:55817-74-8 SDS

55817-74-8Relevant articles and documents

Synthesis of 7-Unsubstituted 7H-Pyrrolopyrimidines

Pichler, Herbert,Folkers, Gerd,Roth, Hermann J.,Eger, Kurt

, p. 1485 - 1505 (2007/10/02)

The title compounds 4 are obtained by N-7 dealkylation of the 2-furanylmethyl, 2-thiophenylmethyl, or 1-phenylethyl group from 2a-g and 10 a-j with polyphosphoric acid.In contrast to the 2-furanylmethyl group the 2-thiophenylmethyl and 1-phenylethyl group

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