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CAS

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132682-08-7

Alanine, 2-methyl-N-[[(phenylmethoxy)carbonyl]-L-leucyl]-, 2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132682-08-7 Structure

  • Basic information

    1. Product Name: Alanine, 2-methyl-N-[[(phenylmethoxy)carbonyl]-L-leucyl]-, 2-propenyl ester
    2. Synonyms:
    3. CAS NO:132682-08-7
    4. Molecular Formula: C21H30N2O5
    5. Molecular Weight: 390.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132682-08-7.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: Alanine, 2-methyl-N-[[(phenylmethoxy)carbonyl]-L-leucyl]-, 2-propenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Alanine, 2-methyl-N-[[(phenylmethoxy)carbonyl]-L-leucyl]-, 2-propenyl ester(132682-08-7)
    11. EPA Substance Registry System: Alanine, 2-methyl-N-[[(phenylmethoxy)carbonyl]-L-leucyl]-, 2-propenyl ester(132682-08-7)

  • 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: 132682-08-7(Hazardous Substances Data)

132682-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132682-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132682-08:
(8*1)+(7*3)+(6*2)+(5*6)+(4*8)+(3*2)+(2*0)+(1*8)=117
117 % 10 = 7
So 132682-08-7 is a valid CAS Registry Number.

132682-08-7Relevant articles and documents

PyBOP and PyBroP: Two reagents for the difficult coupling of the α,α-dialkyl amino acid, Aib

Frerot, Eric,Coste, Jacques,Pantaloni, Antoine,Dufour, Marie-Noelle,Jouin, Patrick

, p. 259 - 270 (2007/10/02)

The difficult coupling of α-aminoisobutyric acid (Aib) was carried out using PyBOP and PyBroP in a comparative study with BOP and BroP. These reagents gave good results under simple conditions (one pot, r.t., 1h). Coded amino acids could be coupled with Aib using PyBOP under standard conditions of peptide synthesis without racemization whereas the coupling of two Aib residues required PyBroP/DMAP. A fragment containing an Aib C-terminal could be coupled without epimerization of the penultimate residue.

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