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CAS

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127927-65-5

(4S,5R)-5-Benzyl-4-dibenzylamino-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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  • 127927-65-5 Structure

  • Basic information

    1. Product Name: (4S,5R)-5-Benzyl-4-dibenzylamino-dihydro-furan-2-one
    2. Synonyms: (4S,5R)-5-Benzyl-4-dibenzylamino-dihydro-furan-2-one
    3. CAS NO:127927-65-5
    4. Molecular Formula:
    5. Molecular Weight: 371.479
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127927-65-5.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: (4S,5R)-5-Benzyl-4-dibenzylamino-dihydro-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5R)-5-Benzyl-4-dibenzylamino-dihydro-furan-2-one(127927-65-5)
    11. EPA Substance Registry System: (4S,5R)-5-Benzyl-4-dibenzylamino-dihydro-furan-2-one(127927-65-5)

  • 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: 127927-65-5(Hazardous Substances Data)

127927-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127927-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127927-65:
(8*1)+(7*2)+(6*7)+(5*9)+(4*2)+(3*7)+(2*6)+(1*5)=155
155 % 10 = 5
So 127927-65-5 is a valid CAS Registry Number.

127927-65-5Downstream Products

127927-65-5Relevant articles and documents

TANDEM ALDOLIZATION / LACTONIZATION / DYOTROPIC REARRANGEMENT OF α-AMINO-ALDEHYDES

Reetz, M.T.,Schmitz, A.,Holdgruen, X.

, p. 5421 - 5424 (1989)

N,N-dibenzyl-protected α-amino-aldehydes 1 undergo non-chelation-controlled aldol additions of 1-phenoxy-1-trimethylsiloxyethylene 2 followed by β-lactone formation and dyotropic rearrangement, all three reactions being catalyzed by MgCl2.The products, 4-substituted 3-amino-χ-lactones 3, are stereochemically pure (de and ee > 99percent).

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