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CAS

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130203-12-2

(S)-1-Cyclohex-1-enyl-2-[(diphenylphosphanyl)-methyl]-pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130203-12-2 Structure

  • Basic information

    1. Product Name: (S)-1-Cyclohex-1-enyl-2-[(diphenylphosphanyl)-methyl]-pyrrolidine
    2. Synonyms:
    3. CAS NO:130203-12-2
    4. Molecular Formula:
    5. Molecular Weight: 349.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130203-12-2.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: (S)-1-Cyclohex-1-enyl-2-[(diphenylphosphanyl)-methyl]-pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-Cyclohex-1-enyl-2-[(diphenylphosphanyl)-methyl]-pyrrolidine(130203-12-2)
    11. EPA Substance Registry System: (S)-1-Cyclohex-1-enyl-2-[(diphenylphosphanyl)-methyl]-pyrrolidine(130203-12-2)

  • 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: 130203-12-2(Hazardous Substances Data)

130203-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130203-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,0 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130203-12:
(8*1)+(7*3)+(6*0)+(5*2)+(4*0)+(3*3)+(2*1)+(1*2)=52
52 % 10 = 2
So 130203-12-2 is a valid CAS Registry Number.

130203-12-2Relevant articles and documents

Palladium-catalyzed asymmetric allylations of chiral enamines bearing phosphine functionality. Effects of anionic counterparts of allylating reagents on asymmetric induction

Hiroi,Abe

, p. 3623 - 3626 (2007/10/02)

Palladium-catalyzed asymmetric allylations of chiral enamines bearing a phosphine group were attempted using various allylating reagents to produce optically active α-allyl carbonyl compounds. The great effects of the anionic counterparts of the allylatin

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