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1H-Pyrrole-2-carbonitrile,4-(aminomethyl)-1-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

590409-84-0

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590409-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 590409-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,0,4,0 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 590409-84:
(8*5)+(7*9)+(6*0)+(5*4)+(4*0)+(3*9)+(2*8)+(1*4)=170
170 % 10 = 0
So 590409-84-0 is a valid CAS Registry Number.

590409-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-aminomethyl-1-methylpyrrole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-Aminomethyl-1-methyl-1H-pyrrole-2-carbonitrile

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:590409-84-0 SDS

590409-84-0Downstream Products

590409-84-0Relevant academic research and scientific papers

Thrombin inhibitors

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Page column 49, (2010/02/06)

Novel five-membered heterocyclic amidines, their preparation and use as competitive inhibitors of trypsin-like serine proteases, especially thrombin and kininogenases such as kallikrein. Pharmaceutical compositions which contain the compounds as active ingredients, and use of the compounds as thrombin inhibitors, anticoagulants and antiinflammatory agents.

D-Phe-Pro-Arg type thrombin inhibitors: Unexpected selectivity by modification of the P1 moiety

Lange, Udo E. W.,Baucke, Dorit,Hornberger, Wilfried,Mack, Helmut,Seitz, Werner,Hoeffken, H. Wolfgang

, p. 2029 - 2033 (2007/10/03)

Synthesis of thrombin inhibitors and their binding mode to thrombin is described. Modification of the P1 moiety leads to an increased selectivity versus trypsin. The observed selectivity is discussed in view of their thrombin-inhibitor complex X-ray struc

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