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ETHYL AZIRIDINYL FORMATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 671-51-2 Structure
  • Basic information

    1. Product Name: ETHYL AZIRIDINYL FORMATE
    2. Synonyms: 1-aziridinecarboxylicacid,ethylester;1-ethoxycarbonylaziridine;ethoxycarbonyl-1-ethylenimine;ethyl1-aziridinecarboxylate;ethyl1-aziridinylcarboxylate;ethylaziridinecarboxylate;ethylaziridinocarboxylate;n-(ethoxycarbonyl)aziridine
    3. CAS NO:671-51-2
    4. Molecular Formula: C5H9NO2
    5. Molecular Weight: 115.13046
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 671-51-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 215.41°C (rough estimate)
    3. Flash Point: 42.8°C
    4. Appearance: /
    5. Density: 1.1808 (rough estimate)
    6. Vapor Pressure: 4.5mmHg at 25°C
    7. Refractive Index: 1.4538 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ETHYL AZIRIDINYL FORMATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ETHYL AZIRIDINYL FORMATE(671-51-2)
    12. EPA Substance Registry System: ETHYL AZIRIDINYL FORMATE(671-51-2)
  • 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: 671-51-2(Hazardous Substances Data)

671-51-2 Usage

Safety Profile

Poison by intravenous andintraperitoneal routes. Mutation data reported. When heated to decomposition it emits toxicfumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 671-51-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 671-51:
(5*6)+(4*7)+(3*1)+(2*5)+(1*1)=72
72 % 10 = 2
So 671-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c1-2-8-5(7)6-3-4-6/h2-4H2,1H3

671-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl aziridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl aziridinylformate

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:671-51-2 SDS

671-51-2Relevant articles and documents

Studies directed toward the synthesis of martinellines : One pot synthesis of pyrroloquinolone ring system

Gurjar, Mukund K.,Pal, Shashwati,Rama Rao

, p. 231 - 234 (2007/10/03)

The Pd-catalysed coupling between aryl iodides and 3-carbethoxy-4,5-dihydropyrroles has been described. With ortho-iodoanilines, tandem cyclisation leading to pyrroloquinolones present in martinellines, was observed.

Process for the production of high energy materials

-

, (2008/06/13)

A process for the production of a high energy nitrate ester involves reacting, in an inert organic solvent, a heterocyclic compound, selected from oxiranes, oxetanes, N-substituted aziridines and N-substituted azetidines, with either N2 O4 or N2 O5, and when the compound is reacted with N2 O4, oxidizing the O- or N-nitrate substituents or substituent in the product to O- or N-nitrate substituent or substituents. The remaining ring carbon atoms on the heterocyclic compound may be substituted or unsubstituted. Preferred substituent groups for the C and/or N ring atoms on the compound include alkyl, cyanoalkyl, haloalkyl, nitroalkyl, and substituted aryl. Several novel nitrate ester are also provided, including nitrated derivatives of polybutadiene, in which between 1% and 25% of the carbon atoms in the polymer are substituted by vicinal nitrate ester (--ONO2) groups.

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