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CAS

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156713-62-1

(3S,6S,7aR)-6-Benzyl-3-isopropyl-6-methyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156713-62-1 Structure

  • Basic information

    1. Product Name: (3S,6S,7aR)-6-Benzyl-3-isopropyl-6-methyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one
    2. Synonyms:
    3. CAS NO:156713-62-1
    4. Molecular Formula:
    5. Molecular Weight: 273.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156713-62-1.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: (3S,6S,7aR)-6-Benzyl-3-isopropyl-6-methyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,6S,7aR)-6-Benzyl-3-isopropyl-6-methyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one(156713-62-1)
    11. EPA Substance Registry System: (3S,6S,7aR)-6-Benzyl-3-isopropyl-6-methyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one(156713-62-1)

  • 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: 156713-62-1(Hazardous Substances Data)

156713-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156713-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156713-62:
(8*1)+(7*5)+(6*6)+(5*7)+(4*1)+(3*3)+(2*6)+(1*2)=141
141 % 10 = 1
So 156713-62-1 is a valid CAS Registry Number.

156713-62-1Relevant articles and documents

Synthesis of Non-Racemic 5,5-Disubstituted 2-Cyclopentenones

Meyers, A. I.,Westrum, Larry J.

, p. 7701 - 7704 (1993)

Chiral, non-racemic, bicyclic lactam 1 (X=Y=H) bearing an angular hydrogen at C-7a (1, R=H), underwent efficient diastereoselective dialkylation producing the quaternary substituted lactams 1 (X=Y=alkyl).The latter were transformed into carbinol amines 5

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