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CAS

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956218-04-5

2-bromo-4-cyanobenzoic acid is a chemical compound with the molecular formula C8H4BrNO2, featuring a benzoic acid core with a bromine atom at the 2-position and a cyano group at the 4-position. This derivative is recognized for its unique structure and reactivity, making it a valuable intermediate in the synthesis of a wide range of chemical products.

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  • 956218-04-5 Structure

  • Basic information

    1. Product Name: 2-bromo-4-cyanobenzoic acid
    2. Synonyms: 2-bromo-4-cyanobenzoic acid
    3. CAS NO:956218-04-5
    4. Molecular Formula: C8H4BrNO2
    5. Molecular Weight: 226.02686
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 956218-04-5.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-bromo-4-cyanobenzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-bromo-4-cyanobenzoic acid(956218-04-5)
    11. EPA Substance Registry System: 2-bromo-4-cyanobenzoic acid(956218-04-5)

  • 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: 956218-04-5(Hazardous Substances Data)

956218-04-5 Usage

Uses

Used in Pharmaceutical Synthesis:
2-bromo-4-cyanobenzoic acid is utilized as a key building block in the development of pharmaceuticals. Its specific functional groups facilitate the creation of new drug molecules, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 2-bromo-4-cyanobenzoic acid serves as an essential component in the synthesis of various agrochemicals. Its incorporation aids in the development of effective compounds for crop protection and enhancement of agricultural yields.
Used in Organic Material Synthesis:
2-bromo-4-cyanobenzoic acid is employed as a precursor in the production of organic materials. Its properties allow for the formation of new materials with specific characteristics, useful in different industrial applications.
Used as a Reagent in Organic Chemistry:
2-bromo-4-cyanobenzoic acid is used as a reagent in organic chemistry reactions, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. Its reactivity makes it instrumental in various research and industrial processes, broadening the scope of chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 956218-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,2,1 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 956218-04:
(8*9)+(7*5)+(6*6)+(5*2)+(4*1)+(3*8)+(2*0)+(1*4)=185
185 % 10 = 5
So 956218-04-5 is a valid CAS Registry Number.

956218-04-5SDS

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 Benzoic acid, 2-?bromo-?4-?cyano-

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:956218-04-5 SDS

956218-04-5Relevant articles and documents

Carboxylate-directed Kumada coupling of an acetaldehyde synthon with 2-bromobenzoates used towards the synthesis of isochromanes

Houpis, Ioannis N.,Van Hoeck, Jean-Pierre,Tilstam, Ulf

, p. 2179 - 2184 (2008/02/10)

This letter describes the Kumada coupling of bromobenzoic acid derivatives with the acetaldehyde enolate synthon (1,3-dioxolan-2-ylmethyl)magnesium bromide. The lithium carboxylate salt shows the highest reactivity in the coupling reaction while addition

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