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187753-87-3

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187753-87-3 Usage

Uses

BU 239 Hydrochloride is a useful research which can be used to compete with benzofuranyl imidazoline radioligand in rat brain for I2 receptors.

Biological Activity

High affinity ligand for the imidazoline I 2 binding site.

Check Digit Verification of cas no

The CAS Registry Mumber 187753-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,7,5 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 187753-87:
(8*1)+(7*8)+(6*7)+(5*7)+(4*5)+(3*3)+(2*8)+(1*7)=193
193 % 10 = 3
So 187753-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N4.ClH/c1-2-4-9-8(3-1)14-7-10(15-9)11-12-5-6-13-11;/h1-4,7H,5-6H2,(H,12,13);1H

187753-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BU 239 hydrochloride,2-(4,5-Dihydroimidazol-2-yl)quinoxalinehydrochloride

1.2 Other means of identification

Product number -
Other names BU 239 HYDROCHLORIDE

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:187753-87-3 SDS

187753-87-3Downstream Products

187753-87-3Relevant articles and documents

Synthesis of substituted aryl amidines from aminoacetonitriles

Yin, Zhiwei,Zhang, Zhongxing,Zhu, Juliang,Wong, Henry,Kadow, John F.,Meanwell, Nicholas A.,Wang, Tao

, p. 4919 - 4923 (2005)

Aryl aminoacetonitriles are oxidized by NiO2-H2O or MnO2 in the presence of a wide range of NH2-containing compounds to afford aryl amidines, presumably via iminium intermediates. A 'one-pot' procedure for the preparation of heteroaryl amidines from N-containing heteroaryl halides through a process comprising sequential SNAr substitution and oxidation has also been developed.

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