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CAS

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180839-81-0

(2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180839-81-0 Structure

  • Basic information

    1. Product Name: (2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde
    2. Synonyms: (2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde
    3. CAS NO:180839-81-0
    4. Molecular Formula:
    5. Molecular Weight: 309.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180839-81-0.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: (2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde(180839-81-0)
    11. EPA Substance Registry System: (2R,3R)-1-Benzyl-3-benzyloxy-2-methyl-4-oxo-azetidine-2-carbaldehyde(180839-81-0)

  • 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: 180839-81-0(Hazardous Substances Data)

180839-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180839-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,8,3 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 180839-81:
(8*1)+(7*8)+(6*0)+(5*8)+(4*3)+(3*9)+(2*8)+(1*1)=160
160 % 10 = 0
So 180839-81-0 is a valid CAS Registry Number.

180839-81-0Relevant articles and documents

Concise synthesis of α-alkyl α-amino acids and their incorporation into peptides via β-lactam-derived α-amino acid N-carboxy anhydrides

Palomo, Claudio,Aizpurua,Ganboa, Inaki,Odriozola, Beatriz,Urchegui, Raquel,Goerls, Helmar

, p. 1269 - 1270 (1996)

a-Hydroxy β-lactams in which C4 exists as a quaternary carbon are transformed in a single one-pot operation into α,α-dialkyl α-amino acid N-carboxy anhydrides providing a new approach to conformationally restricted peptide segments from non α-a

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