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2-Amino-3-bromobenzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114344-60-4

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114344-60-4 Usage

Synthesis Reference(s)

Synthetic Communications, 19, p. 2255, 1989 DOI: 10.1080/00397918908052624

Check Digit Verification of cas no

The CAS Registry Mumber 114344-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,4 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114344-60:
(8*1)+(7*1)+(6*4)+(5*3)+(4*4)+(3*4)+(2*6)+(1*0)=94
94 % 10 = 4
So 114344-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrN2/c8-6-3-1-2-5(4-9)7(6)10/h1-3H,10H2

114344-60-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H61823)  2-Amino-3-bromobenzonitrile, 95%   

  • 114344-60-4

  • 250mg

  • 1142.0CNY

  • Detail
  • Alfa Aesar

  • (H61823)  2-Amino-3-bromobenzonitrile, 95%   

  • 114344-60-4

  • 1g

  • 3627.0CNY

  • Detail

114344-60-4SDS

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 2-Amino-3-bromobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-Bromo-6-cyanoaniline

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:114344-60-4 SDS

114344-60-4Relevant academic research and scientific papers

The components of xRNA: Synthesis and fluorescence of a full genetic set of size-expanded ribonucleosides

Hernandez, Armando R.,Kool, Eric T.

supporting information; experimental part, p. 676 - 679 (2011/05/03)

The synthesis and properties of a full set of four benzo-expanded ribonucleosides (xRNA), analogous to A, G, C, and U RNA monomers, are described. The nucleosides are efficient fluorophores with emission maxima of 369-411 nm. The compounds are expected to

Novel bromination method for anilines and anisoles using NH 4Br/H2O2 in CH3COOH

Krishna Mohan,Narender,Srinivasu,Kulkarni,Raghavan

, p. 2143 - 2152 (2007/10/03)

A simple, efficient, regioselective, environmentally safe, and economical method for the oxybromination of anilines and anisoles without catalyst is reported. The electrophilic substitution of bromine generated in situ from ammonium bromide as a bromine source and hydrogen peroxide as an oxidant for the first time.

Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate

Roche, Didier,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 2083 - 2085 (2007/10/03)

The selective monobromination of various deactivated anilines using potassium bromide and sodium perborate as oxidant has been achieved. The use of ammonium molybdate as catalyst accelerates the rate of reaction but is not essential to obtain good yields and high selectivities. (C) 2000 Elsevier Science Ltd.

Liquid phase regioselective bromination of aromatic compounds over HZSM-5 catalyst

Narender,Srinivasu,Kulkarni,Raghavan

, p. 3669 - 3675 (2007/10/03)

A simple, efficient, regioselective and environmentally safe method for oxybromination of activated aromatics catalyzed by HZSM-5 is reported. The electrophilic substitution of bromine generated from KBr using HZSM-5 as a catalyst and H2O2 as an oxidant.

Certain 1H-pyrrold[3,4-b]quinolin-1-one-9-amino-2,3-dihydro derivatives useful for treating anxiety

-

, (2008/06/13)

The present invention comprises certain quinoline lactams of formula I; pharmaceutically acceptable salts of the compounds of formula I; pharmaceutical compositions containing a compound of formula I, or a pharmaceutically acceptable salt thereof, for use in the treatment of anxiety; and processes for the manufacture of the compounds of formula I, as well as intermediates for use in such manufacture.

SYNTHESIS OF ANTHRANILONITRILES BY FRAGMENTATION OF ISATIN OXIME TRIFLATES

Campbell, James B.,Davenport, Timothy W.

, p. 2255 - 2264 (2007/10/02)

Isatin oxime triflates undergo a facile fragmentaton which is promoted by DBU, to form anthranilonitriles after hydrolytic work-up.

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