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CAS

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135028-04-5

(S)-3-Methyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135028-04-5 Structure

  • Basic information

    1. Product Name: (S)-3-Methyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-butyric acid
    2. Synonyms:
    3. CAS NO:135028-04-5
    4. Molecular Formula:
    5. Molecular Weight: 205.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135028-04-5.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: (S)-3-Methyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-butyric acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-Methyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-butyric acid(135028-04-5)
    11. EPA Substance Registry System: (S)-3-Methyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-butyric acid(135028-04-5)

  • 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: 135028-04-5(Hazardous Substances Data)

135028-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135028-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135028-04:
(8*1)+(7*3)+(6*5)+(5*0)+(4*2)+(3*8)+(2*0)+(1*4)=95
95 % 10 = 5
So 135028-04-5 is a valid CAS Registry Number.

135028-04-5Downstream Products

135028-04-5Relevant articles and documents

N-Amination Using N-Methoxycarbonyl-3-phenyloxaziridine. Direct Access to Chiral Nβ-Protected α-Hydrazinoacids and Carbazates

Vidal, Joelle,Drouin, Jacques,Collet, Andre

, p. 435 - 437 (2007/10/02)

Primary and secondary amines =NH, including α-aminoacids, can be converted under mild conditions to the corresponding carbazates =N-NH-CO2Me, on reaction with N-methoxycarbonyl-3-phenyloxaziridine 1.

α-ALKYLATION OF ACYCLIC AMINO ACIDS WITH SELF-REPRODUCTION OF THE CENTER OF CHIRALITY. A NEW ROUTE TO (S)-(+)-α-ALKYLATED ASPARTIC ACIDS.

Fadel, Antoine,Salaun, Jacques

, p. 2243 - 2246 (2007/10/02)

The amino acids 1a-d (alanine, phenylalanine, valine and methionine) are alkylated by ethyl bromoacetate, with inversion of configuration, to provide readily with high stereoselectivity the α-alkylated aspartic acids 9a-d through the chiral enolates 7a-d

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