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CAS

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60067-08-5

Acetamide, 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methyl-, monohydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60067-08-5 Structure

  • Basic information

    1. Product Name: Acetamide, 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methyl-, monohydrobromide
    2. Synonyms:
    3. CAS NO:60067-08-5
    4. Molecular Formula: C16H15ClN2O2.BrH
    5. Molecular Weight: 383.672
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60067-08-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetamide, 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methyl-, monohydrobromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methyl-, monohydrobromide(60067-08-5)
    11. EPA Substance Registry System: Acetamide, 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methyl-, monohydrobromide(60067-08-5)

  • 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: 60067-08-5(Hazardous Substances Data)

60067-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60067-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60067-08:
(7*6)+(6*0)+(5*0)+(4*6)+(3*7)+(2*0)+(1*8)=95
95 % 10 = 5
So 60067-08-5 is a valid CAS Registry Number.

60067-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methylacetamide hydrobromide

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:60067-08-5 SDS

60067-08-5Downstream Products

60067-08-5Relevant articles and documents

THERAPEUTIC COMPOUNDS AND FORMULATIONS FOR INTRANASAL DELIVERY

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Page/Page column 29-30, (2016/10/24)

Certain embodiments of the invention provide a formulation suitable for nasal administration comprising water, a prodrug of a therapeutic agent, and an enzyme that is suitable for intranasal conversion of the prodrug to the therapeutic agent, as well as methods of use thereof.

Benzophenone glycinamide derivatives

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, (2008/06/13)

This invention is directed toward pharmacologically active compounds of the formula STR1 wherein A represents a nitrogen atom which may be substituted by a methyl, cyclopropylmethyl, di(C1-4 alkyl)aminoethyl, methoxymethyl or hydroxyethyl group and B represents a carbonyl group or A and B together represent a grouping of the formula STR2 in which Ra represents a hydrogen atom or a lower alkyl or hydroxymethyl group and X represents a nitrogen atom or C--Rb wherein Rb represents a hydrogen atom or a lower alkyl or hydroxymethyl group; R represents a halogen atom or a nitro or trifluoromethyl group; R1 represents a hydrogen atom or a lower alkyl group; R2 represents an acyl group derived from a naturally occurring amino acid (all such groups which contain an asymmetric carbon atom having the L- or D,L-configuration) and R3 represents a phenyl, halophenyl or 2-pyridyl group And acid addition salts thereof. Also provided are methods for their preparation and intermediates thereof. These compounds exhibit activity as anticonvulsants, muscle relaxants and sedatives.

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