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103369-09-1

N-(acetoxymethyl)-4-chlorobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103369-09-1 Structure

  • Basic information

    1. Product Name: N-(acetoxymethyl)-4-chlorobenzamide
    2. Synonyms: N-(acetoxymethyl)-4-chlorobenzamide
    3. CAS NO:103369-09-1
    4. Molecular Formula: C10H10ClNO3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103369-09-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 385.3°Cat760mmHg
    3. Flash Point: 186.8°C
    4. Appearance: /
    5. Density: 1.277g/cm3
    6. Vapor Pressure: 3.84E-06mmHg at 25°C
    7. Refractive Index: 1.538
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(acetoxymethyl)-4-chlorobenzamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(acetoxymethyl)-4-chlorobenzamide(103369-09-1)
    12. EPA Substance Registry System: N-(acetoxymethyl)-4-chlorobenzamide(103369-09-1)

  • 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: 103369-09-1(Hazardous Substances Data)

103369-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103369-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,6 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103369-09:
(8*1)+(7*0)+(6*3)+(5*3)+(4*6)+(3*9)+(2*0)+(1*9)=101
101 % 10 = 1
So 103369-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNO3/c1-7(13)15-6-12-10(14)8-2-4-9(11)5-3-8/h2-5H,6H2,1H3,(H,12,14)

103369-09-1SDS

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 [(4-Chlorobenzoyl)amino]methyl acetate

1.2 Other means of identification

Product number -
Other names N-(acetoxymethyl)-4-chloro-benzamide

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:103369-09-1 SDS

103369-09-1Downstream Products

103369-09-1Relevant articles and documents

Acetamides and benzamides that are useful in treating sexual dysfunction

-

, (2008/06/13)

The present invention relates to the use of compounds of formula (I) for the treatment of sexual dysfunction and to compositions containing compounds of formula (I) for the treatment of sexual dysfunction.

Acetamides and benzamides that are useful in treating sexual dysfunction

-

Page 59, (2010/02/06)

The present invention relates to the use of compounds of formula (I) for the treatment of sexual dysfunction and to compositions containing compounds of formula (I) for the treatment of sexual dysfunction.

Acetamides and benzamides that are useful in treating sexual dysfunction

-

Page 83, (2008/06/13)

The present invention relates to the use of compounds of formula (I) for the treatment of sexual dysfunction and to compositions containing compounds of formula (I) for the treatment of sexual dysfunction.

Synthesis of N-(morpholinomethyl) benzamides as moclobemide analogs

Pessoa-Mahana, Hernan,Astudillo, Claudio I. O.,Araya-Maturana

, p. 1437 - 1445 (2007/10/03)

Syntheses of new morpholinomethylbenzamides 6 bearing both electron-withdrawing and electron-releasing groups at the aromatic ring are described. The strategy involved synthesis of hippuric acid ethyl esters 3, their hydrolysis to hippuric acids 4, subseq

The Oxidative Decarboxylation of N-Aroylglycines to N-(Aacetoxymethyl)benzamides and N-Formylbenzamides with Lead(IV) Acetate

Gledhill, Adrian P.,McCall, Carol J.,Threadgill, Michael D.

, p. 3196 - 3201 (2007/10/02)

Treatment of N-aroylglycines that do not bear a strong electron-withdrawing substituents with lead(IV) acetate in acetic acid/acetic anhydride mixtures at 60-100 deg C rapidly gives the corresponding N-(acetoxymethyl)benzamides and N-formylbenzamides in m

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