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CAS

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928853-07-0

Proline, 5-oxo-4-[5-(phenylmethyl)-2H-tetrazol-2-yl]-, 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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  • 928853-07-0 Structure

  • Basic information

    1. Product Name: Proline, 5-oxo-4-[5-(phenylmethyl)-2H-tetrazol-2-yl]-, methyl ester
    2. Synonyms:
    3. CAS NO:928853-07-0
    4. Molecular Formula: C14H15N5O3
    5. Molecular Weight: 301.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 928853-07-0.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: Proline, 5-oxo-4-[5-(phenylmethyl)-2H-tetrazol-2-yl]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Proline, 5-oxo-4-[5-(phenylmethyl)-2H-tetrazol-2-yl]-, methyl ester(928853-07-0)
    11. EPA Substance Registry System: Proline, 5-oxo-4-[5-(phenylmethyl)-2H-tetrazol-2-yl]-, methyl ester(928853-07-0)

  • 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: 928853-07-0(Hazardous Substances Data)

928853-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928853-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,8,5 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 928853-07:
(8*9)+(7*2)+(6*8)+(5*8)+(4*5)+(3*3)+(2*0)+(1*7)=210
210 % 10 = 0
So 928853-07-0 is a valid CAS Registry Number.

928853-07-0Downstream Products

928853-07-0Relevant articles and documents

Synthesis of new tetrazole and triazole substituted pyroglutamic acid and proline derivatives

Lenda, Fatimazohra,Guenoun, Farhate,Martinez, Jean,Lamaty, Frédéric

, p. 805 - 808 (2007/10/03)

Racemic 4-(substituted-1H-1,2,3-triazol-1-yl), 4-aryl and 4-(arylmethyl)tetrazolyl-pyroglutamic and proline derivatives were synthesized from dimethyl-2,4-dibromoglutaryle 1 in good yield using mild reaction conditions. The key step for the preparation of the triazole substituted molecule was the 1,3-dipolar cycloaddition of an acetylenic compound with an azido derivative. The tetrazole derivatives were prepared by the selective N2-alkylation of 5-substituted tetrazoles with 1.

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