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1003025-51-1

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1003025-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1003025-51-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,0,2 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1003025-51:
(9*1)+(8*0)+(7*0)+(6*3)+(5*0)+(4*2)+(3*5)+(2*5)+(1*1)=61
61 % 10 = 1
So 1003025-51-1 is a valid CAS Registry Number.

1003025-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-(4-fluorophenyl)quinazoline

1.2 Other means of identification

Product number -
Other names 4-chloro-6-(4-fluorophenyl)-quinazoline

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:1003025-51-1 SDS

1003025-51-1Upstream product

1003025-51-1Downstream Products

1003025-51-1Relevant articles and documents

Synthesis and in vitro cytotoxicity of the 4-(Halogenoanilino)-6-bromoquinazolines and their 6-(4-fluorophenyl) substituted derivatives as potential inhibitors of epidermal growth factor receptor tyrosine kinase

Mphahlele, Malose Jack,Paumo, Hugues K.,Choong, Yee Siew

, (2017)

Series of the 2-unsubstituted and 2-(4-chlorophenyl)–substituted 4-anilino-6-bromoquinazolines and their 6-(4-fluorophenyl)–substituted derivatives were evaluated for in vitro cytotoxicity against MCF-7 and HeLa cells. The 2-unsubstituted 4-anilino-6-brom

4,6-DL- AND 2,4,6-TRISUBSTITUTED QUINAZOLINE DERIVATIVES USEFUL FOR TREATING VIRAL INFECTIONS

-

Page/Page column 72, (2008/06/13)

This invention provides quinazoline derivatives represented by the structural formula: (I); wherein: R2 is hydrogen, NR'R", C1-7 alkyl, arylC1-7 alkyl or C3-10 cycloalkyl; R4 is amino, C1-7

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