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N-(((4-((5-Bromo-2-pyrimidinyl)oxy)-3-nitrophenyl)amino)carbonyl)-2-ni trobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103829-01-2

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103829-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103829-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103829-01:
(8*1)+(7*0)+(6*3)+(5*8)+(4*2)+(3*9)+(2*0)+(1*1)=102
102 % 10 = 2
So 103829-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H11BrN6O7/c19-10-8-20-18(21-9-10)32-15-6-5-11(7-14(15)25(30)31)22-17(27)23-16(26)12-3-1-2-4-13(12)24(28)29/h1-9H,(H2,22,23,26,27)

103829-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[4-(5-bromopyrimidin-2-yl)oxy-3-nitrophenyl]carbamoyl]-2-nitrobenzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-[[[4-[(5-bromo-2-pyrimidinyl)oxy]-3-nitrophenyl]amino]carbonyl]-2-nitro

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:103829-01-2 SDS

103829-01-2Downstream Products

103829-01-2Relevant academic research and scientific papers

Synthesis and antitumor activities of novel benzoylphenylurea derivatives

Okada,Koyanagi,Yamada,Haga

, p. 2308 - 2315 (2007/10/02)

Seventy novel benzoylphenylurea compounds were synthesized and their antitumor activities were examined in vivo against P388 leukemia. N-(2-Nitrobenzoyl)-N'-[4-(2-pyrimidinyloxy)phenyl]ureas showed the highest antitumor activities when dosed intraperitoneally or orally. Their structure-activity relationships were examined with particular focus on the position and the variety of substituent on each aryl ring.

N-benzoyl-N'-(3-nitrophenyl) urea compounds, and antitumorous compositions containing them

-

, (2008/06/13)

An N-benzoyl-N'-(3-nitrophenyl) urea compound having the formula STR1 wherein each of X1 and X2 is a hydrogen atom, a halogen atom, a trifluoromethyl group or a nitro group, and Y is STR2 (wherein R is a hydrogen atom, a halogen atom

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