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2-BROMOBENZOYL CYANIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88562-26-9 Structure
  • Basic information

    1. Product Name: 2-BROMOBENZOYL CYANIDE
    2. Synonyms: 2-BROMOBENZOYL CYANIDE;2-(2-bromophenyl)-2-oxoacetonitrile;(2-BroMo-phenyl)-oxo-acetonitrile
    3. CAS NO:88562-26-9
    4. Molecular Formula: C8H4BrNO
    5. Molecular Weight: 210.03
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88562-26-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-BROMOBENZOYL CYANIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-BROMOBENZOYL CYANIDE(88562-26-9)
    11. EPA Substance Registry System: 2-BROMOBENZOYL CYANIDE(88562-26-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 88562-26-9(Hazardous Substances Data)

88562-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88562-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88562-26:
(7*8)+(6*8)+(5*5)+(4*6)+(3*2)+(2*2)+(1*6)=169
169 % 10 = 9
So 88562-26-9 is a valid CAS Registry Number.

88562-26-9SDS

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-BROMOBENZOYL CYANIDE

1.2 Other means of identification

Product number -
Other names AB1240

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:88562-26-9 SDS

88562-26-9Relevant articles and documents

INHIBITING UBIQUITIN SPECIFIC PEPTIDASE 9X

-

Paragraph 0073-0074; 0163, (2020/07/15)

The disclosure provides novel chemical compounds useful as inhibitors of ubiquitin specific peptidase 9X (USP9X). USP9X inhibiting compounds are useful in the treatment of disease and disorders associated with modulation of USP9X, such as cancer.

Acceptorless and Base-free Dehydrogenation of Cyanohydrin with (η6-Arene)halide(Bidentate Phosphine)ruthenium(II) Complex

Kim, Kicheol,Moeljadi, Adhitya Mangala Putra,Hirao, Hajime,Hong, Soon Hyeok

, p. 3292 - 3298 (2017/09/06)

Ruthenium-catalyzed dehydrogenation of cyanohydrins under acceptorless and base-free conditions was demonstrated for the first time in the synthesis of acyl cyanide. As opposed to the thermodynamically preferred elimination of hydrogen cyanide, the dehydrogenation of cyanohydrins could be kinetically controlled with ruthenium (II) bidentate phosphine complexes. The effects of the arene, phosphine ligands and counter anions were investigated in regard to catalytic activity and selectivity. Selective dehydrogenation can occur via β-hydride elimination with the experimentally observed [(alkoxide)Ru] complex. (Figure presented.).

Regioselective synthesis of 1-substituted indazole-3-carboxylic acids

Veerareddy, Arava,Gogireddy, Surendrareddy,Dubey

, p. 1311 - 1321 (2015/04/27)

In this article, we study the synthesis of 1-substituted indazole-3-carboxylic acids from 2-halobenzoic acids.

Chemical process

-

, (2008/06/13)

According to the present invention there is provided process for preparing a compound of formula (I): STR1 or a salt, acylate or sulphonate derivative thereof; wherein R1 is an optionally substituted aryl group, R2, R3, R4 and R5 are selected from hydrogen, C1-4 alkyl, C1-4 alkanoyl or --CO2 Ra wherein Ra is C1-4 alkyl or R2 and R3 or R4 and R5 together with the carbon atom to which they are attached form a C3-6 cycloalkyl ring, provided that at least R2 and R3 or R4 and R5 are not both hydrogen and that not more than two of R2, R3, R4 and R5 are C1-4 alkanoyl or --CO2 Ra ; which process comprises reacting a compound of formula (II): STR2 wherein R2, R3, R4 and R5 are as defined in relation to formula (I) with a compound of formula (III): wherein R1 is as defined in relation to formula (I) in the presence of a base and a Lewis acid.

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