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CAS

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165801-06-9

(R)-2-benzyloxy-3,3,3-trifluoropropanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 165801-06-9 Structure

  • Basic information

    1. Product Name: (R)-2-benzyloxy-3,3,3-trifluoropropanol
    2. Synonyms: (R)-2-benzyloxy-3,3,3-trifluoropropanol
    3. CAS NO:165801-06-9
    4. Molecular Formula:
    5. Molecular Weight: 220.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 165801-06-9.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: (R)-2-benzyloxy-3,3,3-trifluoropropanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-benzyloxy-3,3,3-trifluoropropanol(165801-06-9)
    11. EPA Substance Registry System: (R)-2-benzyloxy-3,3,3-trifluoropropanol(165801-06-9)

  • 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: 165801-06-9(Hazardous Substances Data)

165801-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165801-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 165801-06:
(8*1)+(7*6)+(6*5)+(5*8)+(4*0)+(3*1)+(2*0)+(1*6)=129
129 % 10 = 9
So 165801-06-9 is a valid CAS Registry Number.

165801-06-9Relevant articles and documents

Diastereoselective trifluoromethylation of chiral imide enolates with iodotrifluoromethane mediated by triethylborane

Iseki,Nagai,Kobayashi

, p. 961 - 974 (2007/10/02)

The trifluoromethylation of lithium enolates of chiral N-acyloxazolidinones with iodotrifluoromethane mediated by triethylborane proceeds with good diastereomeric excess.

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