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1158080-74-0

C17H16(2)HF3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1158080-74-0 Structure

  • Basic information

    1. Product Name: C17H16(2)HF3O2
    2. Synonyms:
    3. CAS NO:1158080-74-0
    4. Molecular Formula:
    5. Molecular Weight: 311.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1158080-74-0.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: C17H16(2)HF3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H16(2)HF3O2(1158080-74-0)
    11. EPA Substance Registry System: C17H16(2)HF3O2(1158080-74-0)

  • 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: 1158080-74-0(Hazardous Substances Data)

1158080-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158080-74-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,0,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1158080-74:
(9*1)+(8*1)+(7*5)+(6*8)+(5*0)+(4*8)+(3*0)+(2*7)+(1*4)=150
150 % 10 = 0
So 1158080-74-0 is a valid CAS Registry Number.

1158080-74-0Upstream product

1158080-74-0Downstream Products

1158080-74-0Relevant articles and documents

Convenient synthesis of optically active deuterated primary alcohols via deuteride reduction of acetals derived from homochiral (1R*,2R*)-3,3,3-trifluoro-1-phenylpropane-1,2-diols

Morelli, Carlo F.,Cairoli, Paola,Marigolo, Tiziana,Speranza, Giovanna,Manitto, Paolo

, p. 351 - 354 (2009)

(1R)-1-Deuterated alcohols with high enantiomeric excess were prepared via TiCl4/Et3SiD reduction of acetals arising from the reaction of aldehydes with (1S,2S)-3,3,3-trifluoro-1-phenylpropane-1,2-diol 9. Such a chiral auxiliary was

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