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134604-07-2

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134604-07-2 Usage

Chemical Properties

Type of white crystal

Check Digit Verification of cas no

The CAS Registry Mumber 134604-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134604-07:
(8*1)+(7*3)+(6*4)+(5*6)+(4*0)+(3*4)+(2*0)+(1*7)=102
102 % 10 = 2
So 134604-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrN2O2/c8-7-2-1-6(10(11)12)3-5(7)4-9/h1-3H

134604-07-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H55671)  2-Bromo-5-nitrobenzonitrile, 97%   

  • 134604-07-2

  • 1g

  • 181.0CNY

  • Detail
  • Alfa Aesar

  • (H55671)  2-Bromo-5-nitrobenzonitrile, 97%   

  • 134604-07-2

  • 5g

  • 694.0CNY

  • Detail

134604-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-5-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names 1-Cyano-2-bromo-5-nitrobenzene

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:134604-07-2 SDS

134604-07-2Relevant articles and documents

Method for preparing 3,5-disubstituted oxadiazole compound

-

Paragraph 0024; 0029-0030, (2019/04/30)

The invention discloses a method for preparing a 3,5-disubstituted oxadiazole compound N-((3-(2-bromo-5-nitrophenyl)-1,2,4-oxadiazole-5-yl)methyl)ethylamine. 4-nitrobromobenzene used as a starting material undergoes hydroformylation, oximation, eliminatio

Aromatic allylation via diazotization: Metal-free C-C bond formation

Ek, Fredrik,Axelsson, Oskar,Wistrand, Lars-Goeran,Frejd, Torbjoern

, p. 6376 - 6381 (2007/10/03)

A new method for the synthesis of allyl aromatic compounds not involving any metal-containing reagent or catalyst has been developed. Arylamines substituted with a large number of different substituents were converted via diazotizative deamination with tert-butyl nitrite in allyl bromide and acetonitrile to the corresponding allyl aromatic compounds. The allylation reaction was found to be suitable for larger scale synthesis due to short reaction times, a nonextractive workup, and robustness toward moisture, air, and type of solvent.

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