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CAS

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82912-42-3

2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82912-42-3 Structure

  • Basic information

    1. Product Name: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)
    2. Synonyms: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI);tert-butyl aziridine-2-carboxylate
    3. CAS NO:82912-42-3
    4. Molecular Formula: C7H13NO2
    5. Molecular Weight: 143.18
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER
    8. Mol File: 82912-42-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 66 °C(Press: 12 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.049±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 5.76±0.40(Predicted)
    10. CAS DataBase Reference: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(82912-42-3)
    12. EPA Substance Registry System: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(82912-42-3)

  • 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: 82912-42-3(Hazardous Substances Data)

82912-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82912-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,1 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82912-42:
(7*8)+(6*2)+(5*9)+(4*1)+(3*2)+(2*4)+(1*2)=133
133 % 10 = 3
So 82912-42-3 is a valid CAS Registry Number.

82912-42-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl aziridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-AZIRIDINECARBOXYLIC ACID TERT-BUTYL ESTER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82912-42-3 SDS

82912-42-3Downstream Products

82912-42-3Relevant articles and documents

Acyl migration from N to C in aziridine-2-carboxylic esters

Strumfs, Boriss,Hermane, Jekaterina,Belyakov, Sergey,Trapencieris, Peteris

, p. 355 - 362 (2014)

Acyl group migration from N to C in aziridine-2-carboxylates takes place in deprotonation reactions and, as a result, aziridine-2,2-dicarboxylates are formed. Mechanistic studies proved that the observed migration is an intramolecular reaction.

Amine-promoted, organocatalytic aziridination of enones

Armstrong, Alan,Baxter, Carl A.,Lamont, Scott G.,Pape, Andrew R.,Wincewicz, Richard

, p. 351 - 353 (2007/10/03)

(Chemical Equation Presented) A novel method is presented using N-N ylides (prepared by in situ amination of a tertiary amine) for the aziridination of a range of enone systems. The amine may be used sub-stoichiometrically, and promising levels of enantioselectivity are observed with quinine as promoter.

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 (2007/10/03)

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

Amino Acid Synthesis via Ring Opening of N-Sulphonyl Aziridine-2-Carboxylate Esters with Organometallic Reagents.

Baldwin, Jack E.,Spivey, Alan C.,Schofield, Christopher J.,Sweeney, Joseph B.

, p. 6309 - 6330 (2007/10/02)

Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents has been investigated as a method of preparation of optically active amino acids.Key Words: aziridine-2-carboxylate, cuprate, nucleophilic ring opening, amino acid

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