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1H-Imidazole-1-propanenitrile, 4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59626-32-3

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59626-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59626-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59626-32:
(7*5)+(6*9)+(5*6)+(4*2)+(3*6)+(2*3)+(1*2)=153
153 % 10 = 3
So 59626-32-3 is a valid CAS Registry Number.

59626-32-3SDS

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 3-(4-phenylimidazol-1-yl)propanenitrile

1.2 Other means of identification

Product number -
Other names 1H-Imidazole-1-propanenitrile,4-phenyl

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:59626-32-3 SDS

59626-32-3Relevant academic research and scientific papers

Structure based development of phenylimidazole-derived inhibitors of indoleamine 2,3-dioxygenase

Kumar, Sanjeev,Jaller, Daniel,Patel, Bhumika,LaLonde, Judith M.,DuHadaway, James B.,Malachowski, William P.,Prendergast, George C.,Muller, Alexander J.

experimental part, p. 4968 - 4977 (2009/07/11)

Indoleamine 2,3-dioxygenase (IDO) is emerging as an important new therapeutic target for the treatment of cancer, chronic viral infections, and other diseases characterized by pathological immune suppression. With the goal of developing more potent IDO in

Catalysis and regioselectivity in the Michael addition of azoles. Kinetic vs. thermodynamic control

Horvath, Andras

, p. 4423 - 4426 (2007/10/03)

Bicyclic guanidine bases, TBD and MTBD were found to be high]y efficient catalysts in the Michael addition of azoles with α,β-unsaturated nitriles and esters. The factors influencing regioselectivity have been elucidated, and some new azole-Michael adduct

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