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Acetamide, N-(4-chloro-2-formylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53165-18-7 Structure
  • Basic information

    1. Product Name: Acetamide, N-(4-chloro-2-formylphenyl)-
    2. Synonyms:
    3. CAS NO:53165-18-7
    4. Molecular Formula: C9H8ClNO2
    5. Molecular Weight: 197.621
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53165-18-7.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, N-(4-chloro-2-formylphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-(4-chloro-2-formylphenyl)-(53165-18-7)
    11. EPA Substance Registry System: Acetamide, N-(4-chloro-2-formylphenyl)-(53165-18-7)
  • 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: 53165-18-7(Hazardous Substances Data)

53165-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53165-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53165-18:
(7*5)+(6*3)+(5*1)+(4*6)+(3*5)+(2*1)+(1*8)=107
107 % 10 = 7
So 53165-18-7 is a valid CAS Registry Number.

53165-18-7Relevant articles and documents

A general synthesis of novel quinoline-based isoindolin-1-one derivatives

Zhang, Hong,Li, Yang

, p. 2180 - 2189 (2015)

A simple and general one-pot protocol for the synthesis of a series quinoline-based isoindolin-l-ones, namely 7-chloro-2-substituted-2,3-dihydro- 1H-pyrrolo[3,4-b]quinolin-1-ones (5a-p) is described, involving a cascade Williamson-type condensation reacti

Iron-catalyzed aerobic oxidative cleavage of the C-C σ-bond using air as the oxidant: Chemoselective synthesis of carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds

Xing, Qi,Lv, Hui,Xia, Chungu,Li, Fuwei

, p. 489 - 492 (2016/01/12)

A simple iron-catalyzed aerobic oxidative C-C σ-bond cleavage of ketones has been developed. Readily available and environmentally benign air is used as the oxidant. This reaction avoids the use of noble metal catalysts or specialized oxidants, chemoselectively yielding carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds without overoxidation.

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