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CAS

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1577180-45-0

(3R,4S,5S)-1-benzyl-5-cyano-3,4-diacetoxy-2-pyrrolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1577180-45-0 Structure

  • Basic information

    1. Product Name: (3R,4S,5S)-1-benzyl-5-cyano-3,4-diacetoxy-2-pyrrolidinone
    2. Synonyms:
    3. CAS NO:1577180-45-0
    4. Molecular Formula:
    5. Molecular Weight: 316.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1577180-45-0.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: (3R,4S,5S)-1-benzyl-5-cyano-3,4-diacetoxy-2-pyrrolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4S,5S)-1-benzyl-5-cyano-3,4-diacetoxy-2-pyrrolidinone(1577180-45-0)
    11. EPA Substance Registry System: (3R,4S,5S)-1-benzyl-5-cyano-3,4-diacetoxy-2-pyrrolidinone(1577180-45-0)

  • 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: 1577180-45-0(Hazardous Substances Data)

1577180-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1577180-45-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,7,1,8 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1577180-45:
(9*1)+(8*5)+(7*7)+(6*7)+(5*1)+(4*8)+(3*0)+(2*4)+(1*5)=190
190 % 10 = 0
So 1577180-45-0 is a valid CAS Registry Number.

1577180-45-0Upstream product

1577180-45-0Relevant articles and documents

Stereoselective synthesis of 3,4-dihydroxylated prolines and prolinols starting from L -tartaric acid

Oba,Koguchi,Nishiyama

, p. 237 - 243 (2014)

A straightforward and stereoselective synthesis of 3,4-dihydroxyprolines and 3,4-dihydroxyprolinols is described. The key reaction in this synthesis is a protective group-controlled diastereoselective cyanation of a chiral acyliminium intermediate derived from l-tartaric acid. Methanolysis of the obtained cyanolactam gave methyl 3,4-dihydroxypyroglutamate that was converted to 3,4-dihydroxyproline and 3,4-dihydroxyprolinol by reduction of the lactam carbonyl and ester groups in a stepwise manner.

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