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(1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 475271-37-5 Structure
  • Basic information

    1. Product Name: (1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime
    2. Synonyms: (1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime
    3. CAS NO:475271-37-5
    4. Molecular Formula:
    5. Molecular Weight: 305.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 475271-37-5.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: (1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime(475271-37-5)
    11. EPA Substance Registry System: (1E)-1-(2,4-dihydroxy-3,5-dipropylphenyl)-2,2,2-trifluoroethanone oxime(475271-37-5)
  • 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: 475271-37-5(Hazardous Substances Data)

475271-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475271-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,2,7 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 475271-37:
(8*4)+(7*7)+(6*5)+(5*2)+(4*7)+(3*1)+(2*3)+(1*7)=165
165 % 10 = 5
So 475271-37-5 is a valid CAS Registry Number.

475271-37-5Downstream Products

475271-37-5Relevant articles and documents

An efficient synthesis of a dual PPAR α/γ agonist and the formation of a sterically congested α-aryloxyisobutyric acid via a Bargellini reaction

Cvetovich, Raymond J.,Chung, John Y. L.,Kress, Michael H.,Amato, Joseph S.,Matty, Louis,Weingarten, M. David,Tsay, Fuh-Rong,Li, Zhen,Zhou, George

, p. 8560 - 8563 (2005)

A practical synthesis of benzisoxazole 1 and its conversion to α-aryloxyisobutyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed. Benzisoxazole 1 was formed in high yields by the action of either methanesulfonyl chloride/base

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