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176502-69-5

(+/-)-N-benzyl aziridine carboxylate t-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176502-69-5 Structure

  • Basic information

    1. Product Name: (+/-)-N-benzyl aziridine carboxylate t-butyl ester
    2. Synonyms: (+/-)-N-benzyl aziridine carboxylate t-butyl ester
    3. CAS NO:176502-69-5
    4. Molecular Formula:
    5. Molecular Weight: 233.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176502-69-5.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: (+/-)-N-benzyl aziridine carboxylate t-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-N-benzyl aziridine carboxylate t-butyl ester(176502-69-5)
    11. EPA Substance Registry System: (+/-)-N-benzyl aziridine carboxylate t-butyl ester(176502-69-5)

  • 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: 176502-69-5(Hazardous Substances Data)

176502-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176502-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,0 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 176502-69:
(8*1)+(7*7)+(6*6)+(5*5)+(4*0)+(3*2)+(2*6)+(1*9)=145
145 % 10 = 5
So 176502-69-5 is a valid CAS Registry Number.

176502-69-5Relevant articles and documents

Unnatural amino acids. 2. Simple method of obtaining esters of aziridine-2-carboxylic acids by a transesterification reaction

Shtrumfs,Chernyak,Kums,Kalvins,Trapencieris

, p. 725 - 733 (2004)

A series of N-unsubstituted esters of aziridine-2-carboxylic acid has been obtained by transesterification in basic medium using primary, secondary, and tertiary alcohols. Methods of transesterification using various bases (K 2CO3, R

The Ring Opening of Aziridine-2-carboxylate Esters with Organometallic Reagents

Baldwin, Jack E.,Adlington, Robert M.,O'Neil, Ian A.,Schofield, Christopher,Spivey, Alan C.,Sweeney, Joseph B.

, p. 1852 - 1854 (2007/10/02)

The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids.

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