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CAS

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501037-01-0

2-Hexanone, 1,1,1-trifluoro-6-phenoxy-, O-(phenylmethyl)oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501037-01-0 Structure

  • Basic information

    1. Product Name: 2-Hexanone, 1,1,1-trifluoro-6-phenoxy-, O-(phenylmethyl)oxime
    2. Synonyms:
    3. CAS NO:501037-01-0
    4. Molecular Formula: C19H20F3NO2
    5. Molecular Weight: 351.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501037-01-0.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: 2-Hexanone, 1,1,1-trifluoro-6-phenoxy-, O-(phenylmethyl)oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hexanone, 1,1,1-trifluoro-6-phenoxy-, O-(phenylmethyl)oxime(501037-01-0)
    11. EPA Substance Registry System: 2-Hexanone, 1,1,1-trifluoro-6-phenoxy-, O-(phenylmethyl)oxime(501037-01-0)

  • 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: 501037-01-0(Hazardous Substances Data)

501037-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501037-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,3 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 501037-01:
(8*5)+(7*0)+(6*1)+(5*0)+(4*3)+(3*7)+(2*0)+(1*1)=80
80 % 10 = 0
So 501037-01-0 is a valid CAS Registry Number.

501037-01-0Relevant articles and documents

Radical-mediated synthesis of trifluoroethyl amines and trifluoromethyl ketones from alkyl iodides

Kim, Sunggak,Kavali, Rajesh

, p. 7189 - 7191 (2007/10/03)

Radical reaction of alkyl iodides with trifluoromethyl phenylsulfonyl oxime ether 10 and hexamethylditin at 300 nm in benzene afforded the corresponding trifluoromethyl oxime ethers 11 in high yields, which were reduced into the 2,2,2-trifluoroethyl amines with lithium aluminium hydride. The trifluoroethyl amines could be converted into the corresponding trifluoromethyl ketones by treatment with NBS and DBU.

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