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515863-25-9

(S)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 515863-25-9 Structure

  • Basic information

    1. Product Name: (S)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate
    2. Synonyms: (S)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate
    3. CAS NO:515863-25-9
    4. Molecular Formula:
    5. Molecular Weight: 240.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 515863-25-9.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)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate(515863-25-9)
    11. EPA Substance Registry System: (S)-tert-butyl 2-(azidomethyl)-5-oxopyrrolidine-1-carboxylate(515863-25-9)

  • 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: 515863-25-9(Hazardous Substances Data)

515863-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 515863-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,8,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 515863-25:
(8*5)+(7*1)+(6*5)+(5*8)+(4*6)+(3*3)+(2*2)+(1*5)=159
159 % 10 = 9
So 515863-25-9 is a valid CAS Registry Number.

515863-25-9Upstream product

515863-25-9Relevant articles and documents

Diastereoselective synthesis of enantiopure differentially protected cis-4,5-diaminopiperidin-2-one through intramolecular transamidation

Langlois, Nicole

, p. 9531 - 9533 (2007/10/03)

The diastereoselective synthesis of enantiopure differentially protected cis-4,5-diaminopiperidin-2-one was achieved by means of conjugate addition of ammonia to an unsaturated γ-lactam and transamidation reaction with ring expansion as the main steps.

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