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CAS

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426833-07-0

(-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 426833-07-0 Structure

  • Basic information

    1. Product Name: (-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one
    2. Synonyms: (-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one
    3. CAS NO:426833-07-0
    4. Molecular Formula:
    5. Molecular Weight: 284.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 426833-07-0.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: (-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one(426833-07-0)
    11. EPA Substance Registry System: (-)-(2R,3R)-4-benzyloxy-3-hydroxy-2-methyl-1-phenyl-butan-1-one(426833-07-0)

  • 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: 426833-07-0(Hazardous Substances Data)

426833-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 426833-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,8,3 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 426833-07:
(8*4)+(7*2)+(6*6)+(5*8)+(4*3)+(3*3)+(2*0)+(1*7)=150
150 % 10 = 0
So 426833-07-0 is a valid CAS Registry Number.

426833-07-0Relevant articles and documents

Enantioselective monoreduction of 2-alkyl 1,3-diketones using chiral ruthenium catalysts. Synthesis of the C14-C25 fragment of bafilomycin A 1

Eustache, Florence,Dalko, Peter I.,Cossy, Janine

, p. 8823 - 8826 (2007/10/03)

The enantioselective monoreduction of 2-alkyl 1,3-diketones by dynamic kinetic resolution using optically active ruthenium catalysts allowed the preparation of the C14-C25 fragment of bafilomycin A1.

Synthesis of the C14-C25 Subunit of Bafilomycin A1

Eustache, Florence,Dalko, Peter I.,Cossy, Janine

, p. 9994 - 10002 (2007/10/03)

The enantioselective synthesis of the C14-C25 subunit of bafilomycin A 1, was realized in a convergent route. The sequence involves two dynamic kinetic resolution steps of 2-alkyl 1,3-diketones that use optically active ruthenium complexes, an

Enantioselective Monoreduction of 2-Alkyl-1,3-diketones Mediated by Chiral Ruthenium Catalysts. Dynamic Kinetic Resolution

Eustache, Florence,Dalko, Peter I.,Cossy, Janine

, p. 1263 - 1265 (2007/10/03)

(Matrix Presented) The reduction of 2-alkyl-1,3-diketones using (R,R)- or (S,S)-RuCl[N-(tosyl)-1,2-diphenylethylenediamine](p-cymene) in the presence of formic acid and triethylamine affords syn-2-alkyl-3-hydroxy ketones as the major products with high en

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