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CAS

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249622-09-1

(-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 249622-09-1 Structure

  • Basic information

    1. Product Name: (-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane
    2. Synonyms: (-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane
    3. CAS NO:249622-09-1
    4. Molecular Formula:
    5. Molecular Weight: 327.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 249622-09-1.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: (-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane(249622-09-1)
    11. EPA Substance Registry System: (-)-(1R,2R)-2-N,N-dimethylamino-1-ethoxycarbonylmethoxy-1,2-diphenylethane(249622-09-1)

  • 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: 249622-09-1(Hazardous Substances Data)

249622-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 249622-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,9,6,2 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 249622-09:
(8*2)+(7*4)+(6*9)+(5*6)+(4*2)+(3*2)+(2*0)+(1*9)=151
151 % 10 = 1
So 249622-09-1 is a valid CAS Registry Number.

249622-09-1Relevant articles and documents

Studies aimed at enhancement of reactivity and enantioselectivity of a lithium ester enolate using a chiral tridentate lithium amide

Hussein, Mostafa Ahmed,Iida, Akira,Tomioka, Kiyoshi

, p. 11219 - 11228 (1999)

Tridentate chiral amines 7-13 mediated the asymmetric condensation reaction of lithium ester enolate 2 with benzaldehyde p-anisidine imine 3 giving the corresponding β-lactam 4 in up to 75% ee. It became apparent that coexistence of 2 and chiral lithium a

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