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2-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90562-45-1 Structure
  • Basic information

    1. Product Name: 2-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide
    2. Synonyms: 2-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide;2-chloro-N-(2-methylsulfanylphenyl)ethanamide;IVK/0049166;ZINC03245208
    3. CAS NO:90562-45-1
    4. Molecular Formula: C9H10ClNOS
    5. Molecular Weight: 215.7
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90562-45-1.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-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide(90562-45-1)
    11. EPA Substance Registry System: 2-Chloro-N-(2-methylsulfanyl-phenyl)-acetamide(90562-45-1)
  • 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: 90562-45-1(Hazardous Substances Data)

90562-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90562-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,6 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90562-45:
(7*9)+(6*0)+(5*5)+(4*6)+(3*2)+(2*4)+(1*5)=131
131 % 10 = 1
So 90562-45-1 is a valid CAS Registry Number.

90562-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-(2-methylsulfanylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names Chlor-essigsaeure-(2-methylmercapto-anilid)

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:90562-45-1 SDS

90562-45-1Downstream Products

90562-45-1Relevant articles and documents

Synthesis, polarity, and structure of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides

Ishmaeva,Alimova,Vereshchagina, Ya. A.,Chachkov,Artyushin,Sharova

, p. 943 - 946 (2015)

Conformations of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides have been studied by the dipole moment method and quantum chemical calculations. 2-(Diphenylthiophosphoryl)-N-[2-(methylsulfanyl)

Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase

De La Rosa, Martha,Kim, Hong Woo,Gunic, Esmir,Jenket, Cheryl,Boyle, Uyen,Koh, Yung-hyo,Korboukh, Ilia,Allan, Matthew,Zhang, Weijian,Chen, Huanming,Xu, Wen,Nilar, Shahul,Yao, Nanhua,Hamatake, Robert,Lang, Stanley A.,Hong, Zhi,Zhang, Zhijun,Girardet, Jean-Luc

, p. 4444 - 4449 (2007/10/03)

A new series of 1,2,4-triazoles was synthesized and tested against several NNRTI-resistant HIV-1 isolates. Several of these compounds exhibited potent antiviral activities against efavirenz- and nevirapine-resistant viruses, containing K103N and/or Y181C mutations or Y188L mutation. Triazoles were first synthesized from commercially available substituted phenylthiosemicarbazides, then from isothiocyanates, and later by condensing the desired substituted anilines with thiosemicarbazones.

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