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109513-33-9

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109513-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109513-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109513-33:
(8*1)+(7*0)+(6*9)+(5*5)+(4*1)+(3*3)+(2*3)+(1*3)=109
109 % 10 = 9
So 109513-33-9 is a valid CAS Registry Number.

109513-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-6-nitrobenzylidene(p-dimethylaminophenyl)amine N-Oxide

1.2 Other means of identification

Product number -
Other names -

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:109513-33-9 SDS

109513-33-9Relevant academic research and scientific papers

Design of triple helix forming C-glycoside molecules

Li, Jian-Sen,Fan, Yun-Hua,Zhang, Yi,Marky, Luis A.,Gold, Barry

, p. 2084 - 2093 (2007/10/03)

The modeling, synthesis, and characterization of oligomers containing 2-aminoquinazolin-5-yl 2′-deoxynucleotide residues are reported. The 2-aminoquinazoline residues sequence specifically bind via Hoogsteen base pairing as a third strand in the center of

Polyaza heterocycles. Part 3. Halogenation of 1-substituted quinoxalinocinnolines: mechanistic implications

Harvey, Ian W.,Smith, David M.,White, Charles R.

, p. 1699 - 1704 (2007/10/03)

Since it has been proposed that halogenation of quinoxalinocinnolines at C-10, using hydrogen chloride or bromide in chloroform, occurs through initial protonation of the substrate at N-12, attempts have been made to inhibit this protonation by the introduction of an additional substituent at C-1.Where this substituent is chloro, bromo or methyl, chlorination still occurs preferentially at C-10, although the yield and the reaction rate decrease along the series, lending weight to the mechanistic proposal.

Acid-catalysed Cyclisation of o-Sulphonamido Ketene Dithioacetal S-Oxides: A Novel Synthesis of the Indole Ring System

Hewson, Alan T.,Hughes, Kevin,Richardson, Steward K.,Sharpe, David A.,Wadsworth, Alan H.

, p. 1565 - 1569 (2007/10/02)

Treatment of o-sulphonamido aryl ketene dithioacetal S-oxides with hydrochloric acid in the presence of hydrogen sulphide gives 2-methylthioindoles.

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