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benzo[h]isoquinoline-6-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82649-92-1

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82649-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82649-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,4 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82649-92:
(7*8)+(6*2)+(5*6)+(4*4)+(3*9)+(2*9)+(1*2)=161
161 % 10 = 1
So 82649-92-1 is a valid CAS Registry Number.

82649-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[h]isoquinoline-6-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Azaphenanthren-6-carbonitril

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:82649-92-1 SDS

82649-92-1Downstream Products

82649-92-1Relevant academic research and scientific papers

Synthesis and evaluation of substituted benzoisoquinolinones as potent inhibitors of Chk1 kinase

Garbaccio, Robert M.,Huang, Shaei,Tasber, Edward S.,Fraley, Mark E.,Yan, Youwei,Munshi, Sanjeev,Ikuta, Mari,Kuo, Lawrence,Kreatsoulas, Constanine,Stirdivant, Steve,Drakas, Bob,Rickert, Keith,Walsh, Eileen S.,Hamilton, Kelly A.,Buser, Carolyn A.,Hardwick, James,Mao, Xianzhi,Beck, Stephen C.,Abrams, Marc T.,Tao, Weikang,Lobell, Rob,Sepp-Lorenzino, Laura,Hartman, George D.

, p. 6280 - 6285 (2008/03/13)

From HTS lead 1, a novel benzoisoquinolinone class of ATP-competitive Chk1 inhibitors was devised and synthesized via a photochemical route. Using X-ray crystallography as a guide, potency was rapidly enhanced through the installation of a tethered basic

Pyridyl-substituted Cyclobutanes via Photodimerisation of Azastilbenes

Horner, Michael,Huenig, Siegfried

, p. 1183 - 1210 (2007/10/02)

Mono- and diazastilbenes A1 - A9 as well as their mono- and dihydro- or -alkyl quaternary salts are irradiated (UV).Mono salts are smoothly converted into cyclobutanes C in crystalline state and/or in solution.The free bases A or their bis salts, reacting in solution only, from partly or exclusively different products.Their structures together with the constitutions and configurations of the cyclobutanes A are elucidated.Results from the literature are partly confirmed and partly corrected.

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