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132056-17-8

L-Alanine, N-ethylidene- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132056-17-8 Structure

  • Basic information

    1. Product Name: L-Alanine, N-ethylidene- (9CI)
    2. Synonyms: L-Alanine, N-ethylidene- (9CI)
    3. CAS NO:132056-17-8
    4. Molecular Formula: C5H9NO2
    5. Molecular Weight: 115.13046
    6. EINECS: N/A
    7. Product Categories: GLYCINESCAFFOLD
    8. Mol File: 132056-17-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: L-Alanine, N-ethylidene- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Alanine, N-ethylidene- (9CI)(132056-17-8)
    11. EPA Substance Registry System: L-Alanine, N-ethylidene- (9CI)(132056-17-8)

  • 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: 132056-17-8(Hazardous Substances Data)

132056-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132056-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,5 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132056-17:
(8*1)+(7*3)+(6*2)+(5*0)+(4*5)+(3*6)+(2*1)+(1*7)=88
88 % 10 = 8
So 132056-17-8 is a valid CAS Registry Number.

132056-17-8Downstream Products

132056-17-8Relevant articles and documents

Thermally induced oxidative decarboxylation of copper complexes of amino acids and formation of strecker aldehyde

Nashalian, Ossanna,Yaylayan, Varoujan A.

, p. 8518 - 8523 (2015/04/22)

In the Maillard reaction, independent degradations of amino acids play an important role in the generation of amino-acid-specific products, such as Strecker aldehydes or their Schiff bases. Such oxidative decarboxylation reactions are expected to be enhan

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