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CAS

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38484-81-0

L-Aspartic acid, 3-amino-, (3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38484-81-0 Structure

  • Basic information

    1. Product Name: L-Aspartic acid, 3-amino-, (3S)-
    2. Synonyms:
    3. CAS NO:38484-81-0
    4. Molecular Formula: C4H8N2O4
    5. Molecular Weight: 148.119
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38484-81-0.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: L-Aspartic acid, 3-amino-, (3S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Aspartic acid, 3-amino-, (3S)-(38484-81-0)
    11. EPA Substance Registry System: L-Aspartic acid, 3-amino-, (3S)-(38484-81-0)

  • 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: 38484-81-0(Hazardous Substances Data)

38484-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38484-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,8 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38484-81:
(7*3)+(6*8)+(5*4)+(4*8)+(3*4)+(2*8)+(1*1)=150
150 % 10 = 0
So 38484-81-0 is a valid CAS Registry Number.

38484-81-0Relevant articles and documents

Asymmetric Oxidative Dimerization of the Enolates of N-[Bis(methylthio)methylene]- and N-(Diphenylmethylene)glycine Esters

Alvarez-Ibarra, Carlos,Csák?, Aurelio G.,Colmenero, Belén,Quiroga, M. Luz

, p. 2478 - 2482 (1997)

The oxidative dimerization of glycinates 1 with iodine takes place under kinetic control. The stereochemistry of the resulting 3-aminoaspartate 3 depends on the method used (base/solvent) to generate the corresponding enolate 2. Under suitable conditions, high yields and diastereomeric excesses in favor of the threo derivatives 3-I, which have C2 symmetry, were obtained. In the presence of 8-phenylmenthol as chiral auxiliary (25, 3S)-3-aminoaspartic acid 5-I was synthesized.

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