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363620-48-8

N-(4-bromo-2-methylphenyl)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 363620-48-8 Structure

  • Basic information

    1. Product Name: N-(4-bromo-2-methylphenyl)butanamide
    2. Synonyms: N-(4-bromo-2-methylphenyl)butanamide
    3. CAS NO:363620-48-8
    4. Molecular Formula: C11H14BrNO
    5. Molecular Weight: 256.13896
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 363620-48-8.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: N-(4-bromo-2-methylphenyl)butanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-bromo-2-methylphenyl)butanamide(363620-48-8)
    11. EPA Substance Registry System: N-(4-bromo-2-methylphenyl)butanamide(363620-48-8)

  • 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: 363620-48-8(Hazardous Substances Data)

363620-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 363620-48-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,6,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 363620-48:
(8*3)+(7*6)+(6*3)+(5*6)+(4*2)+(3*0)+(2*4)+(1*8)=138
138 % 10 = 8
So 363620-48-8 is a valid CAS Registry Number.

363620-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Bromo-2-methylphenyl)butanamide

1.2 Other means of identification

Product number -
Other names N-(4-bromo-2-methylphenyl)butyramide

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:363620-48-8 SDS

363620-48-8Upstream product

363620-48-8Relevant articles and documents

PROCESS AND INTERMEDIATES FOR THE PREPARATION OF BENZIMIDAZOLECARBOXYLIC ACIDS

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Page/Page column 7; 8, (2011/01/12)

Substituted benzimidazolecarboxylic acids of formula (I), wherein R1 and R2 independently are hydrogen, C1-6 alkyl or C3-6 cycloalkyl, are prepared in a four-step synthesis starting from N-acyl-4-haloanilines of formula (II), wherein R1 is as defined above, R3 is C1-4 alkyl and X is chlorine or bromine.

PROCESS FOR THE PREPARATION OF BENZIMIDAZOLES

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Page/Page column 7, (2011/01/12)

Substituted benzimidazoles of formula (I), wherein R1 and R2 independently are hydrogen, C1-6 alkyl or C3-6 cycloalkyl and R3 is cyano or carboxy, are prepared in a multistep synthesis starting from Ν-acyl-4-halo- anilines of formula (II), wherein R1 and R2 are as defined above and X is chlorine or bromine.

SUBSTITUTED ANILINE DERIVATIVES

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Page 60, (2008/06/13)

The present invention relates to aniline derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.

Method for producing n-butyryl-4-amino-3-methyl-methyl benzoate and the novel compound n-(4-bromine-2-methylphenyl)-butanamide

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, (2008/06/13)

According to the invention, N-butyryl-4amino-3-methyl-methyl benzoate is obtained in a particularly advantageous manner by, initially, reacting o-toluidine with butyric acid chloride, by brominating the reaction product and by reacting the bromide obtaine

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