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1030379-63-5

(2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1030379-63-5 Structure

  • Basic information

    1. Product Name: (2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol
    2. Synonyms: (2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol
    3. CAS NO:1030379-63-5
    4. Molecular Formula:
    5. Molecular Weight: 221.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1030379-63-5.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: (2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol(1030379-63-5)
    11. EPA Substance Registry System: (2S,3R)-N-benzyl-2-amino-5-hexen-1,3-diol(1030379-63-5)

  • 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: 1030379-63-5(Hazardous Substances Data)

1030379-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1030379-63-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,3,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1030379-63:
(9*1)+(8*0)+(7*3)+(6*0)+(5*3)+(4*7)+(3*9)+(2*6)+(1*3)=115
115 % 10 = 5
So 1030379-63-5 is a valid CAS Registry Number.

1030379-63-5Relevant articles and documents

Asymmetric synthesis of cis-4- and trans-3-hydroxypipecolic acids

Alegret, Carlos,Ginesta, Xavier,Riera, Antoni

, p. 1789 - 1796 (2008)

Enantioselective syntheses of cis-4- and trans-3-hydroxypipecolic acids from 2,3-epoxy-5-hexen-1-ol (7) are described. Regioselective C-3 or C-2 ring opening of the epoxide by the appropriate nitrogen nucleophile is the key step in each route. As enantiom

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