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CAS

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792909-07-0

(3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 792909-07-0 Structure

  • Basic information

    1. Product Name: (3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one
    2. Synonyms: (3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one
    3. CAS NO:792909-07-0
    4. Molecular Formula:
    5. Molecular Weight: 192.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 792909-07-0.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: (3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one(792909-07-0)
    11. EPA Substance Registry System: (3S,4R,5S)-3-hydroxy-4-methyl-5-phenyl-dihydro-furan-2-one(792909-07-0)

  • 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: 792909-07-0(Hazardous Substances Data)

792909-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 792909-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,9,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 792909-07:
(8*7)+(7*9)+(6*2)+(5*9)+(4*0)+(3*9)+(2*0)+(1*7)=210
210 % 10 = 0
So 792909-07-0 is a valid CAS Registry Number.

792909-07-0Downstream Products

792909-07-0Relevant articles and documents

Highly diastereo- and enantioselective reactions of enecarbamates with an aldehyde

Matsubara, Ryosuke,Vital, Paulo,Nakamura, Yoshitaka,Kiyohara, Hiroshi,Kobayashi, Shu

, p. 9769 - 9784 (2004)

Catalytic asymmetric addition reactions of enecarbamates with ethyl glyoxylate have been developed using CuClO4·4CH3CN and a diimine ligand as the catalyst. Highly diastereo- and enantioselective addition reactions of α-mono-substitu

METHOD OF ENANTIOMETRICALLY SELECTIVE NUCLEOPHILIC ADDITION REACTION TO CARBONYL OF ENAMIDE AND METHOD OF SYNTHESIZING OPTICALLY ACTIVE ALPHA-HYDROXY-GAMMA-KETO ACID ESTER AND HYDROXYDIKETONE

-

Page/Page column 21-22, (2008/06/13)

A method of an enantioselective nucleophilic addition reaction to carbonyl, which enables an asymmetric synthesis of an optically active α-hydroxy-γ-keto acid ester, an optically active α-hydroxy-γ-amino acid ester, hydroxydiketone compounds, etc. being u

Highly diastereo- and enantioselective reactions of enecarbamates with ethyl glyoxylate to give optically active syn and anti α-alkyl-β- hydroxy imines and ketones

Matsubara, Ryosuke,Nakamura, Yoshitaka,Kobayashi, Shu

, p. 3258 - 3260 (2007/10/03)

The remarkably selective addition of enecarbamates 2 to ethyl glyoxylate (1) in the presence of a copper-dilmine catalyst (0.1 mol%) gives the corresponding imines 3 in high yields with excellent enantioselectivities. A concerted aza-enetype reaction mech

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