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1385877-82-6

benzyl (2S,4R)-4-formyl-2-phenylpyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1385877-82-6 Structure

  • Basic information

    1. Product Name: benzyl (2S,4R)-4-formyl-2-phenylpyrrolidine-1-carboxylate
    2. Synonyms:
    3. CAS NO:1385877-82-6
    4. Molecular Formula:
    5. Molecular Weight: 309.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1385877-82-6.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: benzyl (2S,4R)-4-formyl-2-phenylpyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl (2S,4R)-4-formyl-2-phenylpyrrolidine-1-carboxylate(1385877-82-6)
    11. EPA Substance Registry System: benzyl (2S,4R)-4-formyl-2-phenylpyrrolidine-1-carboxylate(1385877-82-6)

  • 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: 1385877-82-6(Hazardous Substances Data)

1385877-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1385877-82-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,5,8,7 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1385877-82:
(9*1)+(8*3)+(7*8)+(6*5)+(5*8)+(4*7)+(3*7)+(2*8)+(1*2)=226
226 % 10 = 6
So 1385877-82-6 is a valid CAS Registry Number.

1385877-82-6Downstream Products

1385877-82-6Relevant articles and documents

Enantioselective organo-SOMO cycloadditions: A catalytic approach to complex pyrrolidines from olefins and aldehydes

Jui, Nathan T.,Garber, Jeffrey A.O.,Finelli, Fernanda Gadini,MacMillan, David W.C.

, p. 11400 - 11403 (2012/09/05)

A new method to rapidly generate pyrrolidines via a SOMO-activated enantioselective (3 + 2) coupling of aldehydes and conjugated olefins has been accomplished. A radical-polar crossover mechanism is proposed wherein olefin addition to a transient enamine

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