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487058-78-6

5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 487058-78-6 Structure

  • Basic information

    1. Product Name: 5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE
    2. Synonyms: 5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE
    3. CAS NO:487058-78-6
    4. Molecular Formula: C11H12Cl2O
    5. Molecular Weight: 231.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 487058-78-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 348.475°C at 760 mmHg
    3. Flash Point: 147.142°C
    4. Appearance: /
    5. Density: 1.192g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.531
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE(487058-78-6)
    12. EPA Substance Registry System: 5-CHLORO-1-(3-CHLOROPHENYL)-1-OXOPENTANE(487058-78-6)

  • 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: 487058-78-6(Hazardous Substances Data)

487058-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 487058-78-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,7,0,5 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 487058-78:
(8*4)+(7*8)+(6*7)+(5*0)+(4*5)+(3*8)+(2*7)+(1*8)=196
196 % 10 = 6
So 487058-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12Cl2O/c12-7-2-1-6-11(14)9-4-3-5-10(13)8-9/h3-5,8H,1-2,6-7H2

487058-78-6Upstream product

487058-78-6Downstream Products

487058-78-6Relevant articles and documents

Copper-catalyzed radical ring-opening halogenation with HX

Bai, Ming,Duan, Xin-Hua,Guo, Li-Na,Liu, Shuai,Sun, Qing-Xin,Xu, Peng-Fei

supporting information, p. 8652 - 8655 (2021/09/04)

An efficient copper-catalyzed radical ring-opening halogenation with HX (aq) is described. This protocol features redox-neutral conditions, green halogen sources, and a broad substrate scope, providing practical access to distally chlorinated, brominated and iodinated alkyl ketones and alkyl nitriles with moderate to good yields. This journal is

Regioselective Synthesis of Carbonyl-Containing Alkyl Chlorides via Silver-Catalyzed Ring-Opening Chlorination of Cycloalkanols

Huang, Feng-Qing,Xie, Jian,Sun, Jian-Guo,Wang, Yue-Wei,Dong, Xin,Qi, Lian-Wen,Zhang, Bo

supporting information, p. 684 - 687 (2016/03/01)

A novel and regioselective approach to carbonyl-containing alkyl chlorides via silver-catalyzed ring-opening chlorination of cycloalkanols is reported. Concurrent C(sp3)-C(sp3) bond cleavage and C(sp3)-Cl bond formation efficiently occur with good yields under mild conditions, and the chlorinated products are readily transformed into other useful synthetic intermediates and drugs. The reaction features complete regioselectivity, high efficiency, and excellent practicality. (Chemical Equation Presented).

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