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CAS

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38449-08-0

(RS)-N-benzoylleucine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38449-08-0 Structure

  • Basic information

    1. Product Name: (RS)-N-benzoylleucine methyl ester
    2. Synonyms: (RS)-N-benzoylleucine methyl ester
    3. CAS NO:38449-08-0
    4. Molecular Formula:
    5. Molecular Weight: 249.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38449-08-0.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: (RS)-N-benzoylleucine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (RS)-N-benzoylleucine methyl ester(38449-08-0)
    11. EPA Substance Registry System: (RS)-N-benzoylleucine methyl ester(38449-08-0)

  • 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: 38449-08-0(Hazardous Substances Data)

38449-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38449-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38449-08:
(7*3)+(6*8)+(5*4)+(4*4)+(3*9)+(2*0)+(1*8)=140
140 % 10 = 0
So 38449-08-0 is a valid CAS Registry Number.

38449-08-0Downstream Products

38449-08-0Relevant articles and documents

Reaction of N-Benzoyl Amino Acids with Oxalyl Chloride: a Facile Route to 4-Substituted 2-Phenyloxazole-5-carboxylates

Cynkowski, Tadeusz,Cynkowska, Grazyna,Ashton, Paul,Crooks, Peter A.

, p. 2335 - 2336 (2007/10/02)

N-benzoyl amino acids 1a-g react with excess oxalyl chloride at room temperature followed by addition of alcohols to afford 4-substituted 2-phenyloxazole-5-carboxylates 3a-g.

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