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3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester

    Cas No: 95061-50-0

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  • 95061-50-0 Structure
  • Basic information

    1. Product Name: 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester
    2. Synonyms: 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester
    3. CAS NO:95061-50-0
    4. Molecular Formula:
    5. Molecular Weight: 404.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95061-50-0.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: 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester(95061-50-0)
    11. EPA Substance Registry System: 3-Hydroxy-hexanoic acid (R)-2-hydroxy-1,2,2-triphenyl-ethyl ester(95061-50-0)
  • 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: 95061-50-0(Hazardous Substances Data)

95061-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95061-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95061-50:
(7*9)+(6*5)+(5*0)+(4*6)+(3*1)+(2*5)+(1*0)=130
130 % 10 = 0
So 95061-50-0 is a valid CAS Registry Number.

95061-50-0Relevant articles and documents

Stereoselective Aldol Reactions with (R)- and (S)-2-Hydroxy-1,2,2-triphenylethyl Acetate and Related Glycol Monoacetates

Devant, Ralf,Mahler, Ulrike,Braun, Manfred

, p. 397 - 406 (2007/10/02)

The enolate 7a, formed by double deprotonation of the ester 5a, is added to aldehydes.The influences of the enolate gegenion, of the solvent, and of the reaction temperature on the ratio of the isomeric products 9:10 are studied.The highest degrees of dia

(R)- AND (S)-2-ACETOXY-1,1,2-TRIPHENYLETHANOL - EFFECTIVE SYNTHETIC EQUIVALENTS OF A CHIRAL ACETATE ENOLATE

Braun, Manfred,Devant, Ralf

, p. 5031 - 5034 (2007/10/02)

The enolate 3, easily available by double deprotonation of (R)-2-acetoxy-1,1,2-triphenylethanol (5), adds in a highly stereoselective manner to aldehides.Hydrolysis of the adducts 6/7 affods the acids 2.

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