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CAS

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220573-03-5

Benzyl-((1R,4R)-4-hydroxy-cyclohex-2-enyl)-carbamic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220573-03-5 Structure

  • Basic information

    1. Product Name: Benzyl-((1R,4R)-4-hydroxy-cyclohex-2-enyl)-carbamic acid benzyl ester
    2. Synonyms:
    3. CAS NO:220573-03-5
    4. Molecular Formula:
    5. Molecular Weight: 337.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220573-03-5.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-((1R,4R)-4-hydroxy-cyclohex-2-enyl)-carbamic acid benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzyl-((1R,4R)-4-hydroxy-cyclohex-2-enyl)-carbamic acid benzyl ester(220573-03-5)
    11. EPA Substance Registry System: Benzyl-((1R,4R)-4-hydroxy-cyclohex-2-enyl)-carbamic acid benzyl ester(220573-03-5)

  • 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: 220573-03-5(Hazardous Substances Data)

220573-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220573-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,5,7 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220573-03:
(8*2)+(7*2)+(6*0)+(5*5)+(4*7)+(3*3)+(2*0)+(1*3)=95
95 % 10 = 5
So 220573-03-5 is a valid CAS Registry Number.

220573-03-5Relevant articles and documents

An enantio- and diastereoselective synthesis of (-)-isoretronecanol and (+)-trachelanthamidine from a meso precursor

Konno, Hiroyuki,Kishi, Masayo,Hiroya, Kou,Ogasawara, Kunio

, p. 33 - 37 (2007/10/03)

Two diastereomeric pyrrolizidine alkaloids, (-)-isoretronecanol and (+)- trachelanthamidine, have been synthesized in an enantio- and diastereoselective manner starting from a meso precursor via a catalytic asymmetrization.

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