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891782-65-3

2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 891782-65-3 Structure

  • Basic information

    1. Product Name: 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester
    2. Synonyms: 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester
    3. CAS NO:891782-65-3
    4. Molecular Formula: C10H10ClN3O3
    5. Molecular Weight: 255.66
    6. EINECS: N/A
    7. Product Categories: Aromatics Compounds;Aromatics
    8. Mol File: 891782-65-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: Chloroform, Dichloromethane
    9. CAS DataBase Reference: 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester(891782-65-3)
    11. EPA Substance Registry System: 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester(891782-65-3)

  • 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: 891782-65-3(Hazardous Substances Data)

891782-65-3 Usage

Chemical Properties

Colourless Oil

Check Digit Verification of cas no

The CAS Registry Mumber 891782-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,7,8 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 891782-65:
(8*8)+(7*9)+(6*1)+(5*7)+(4*8)+(3*2)+(2*6)+(1*5)=223
223 % 10 = 3
So 891782-65-3 is a valid CAS Registry Number.

891782-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Azido-1-(chloromethyl)ethyl Carbonic Acid Phenyl Ester

1.2 Other means of identification

Product number -
Other names -

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:891782-65-3 SDS

891782-65-3Downstream Products

891782-65-3Relevant articles and documents

PROCESSES FOR THE PREPARATION OF 4-{4-[5(S)-(AMINOMETHYL)-2-OXO-1,3-OXAZOLIDIN-3-YL]PHENYL} MORPHOLIN-3-ONE

-

Page/Page column 18, (2013/03/26)

The present invention provides simple, eco-friendly, cost-effective, reproducible, robust and industrial processes for the preparation of intermediate compound 4-{4-[5(S)-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one (II). The present invention also provides novel intermediates and their use in the synthesis of morpholinone oxazolidine derivatives.

A facile synthesis of 2-((5R)-2-oxo-5-oxazolidinyl)methyl-1H-isoindole-1, 3(2H)-dione

Madhusudhan,Ready, G. Om,Ramanatham,Dubey

, p. 1264 - 1268 (2007/10/03)

Synthesis of enantiomerically pure 2-((5A)-2-oxo-5-oxazolidinyl) methyl)-1H-isoindole-1,3(2H)-dione, a key precursor in the preparation of oxazolidinone class of antibacterial agents starting from (S)-epichlorohydrin has been achieved.

A novel and short convergent approach for N-aryl-5-aminomethyl-2- oxazolidinone derivatives Linezolid and DUP-721

Madhusudhan,Om Reddy,Ramanatham,Dubey

, p. 1236 - 1238 (2007/10/03)

A new convergent and short approach for oxazolidinone class of antibacterial agents, Linezolid and DUP-721, has been achieved by condensing 3-chloro-2-((phenoxycarbonyl)oxy) propyl azide with aryl amine followed by reductive acetylation. This one pot approach for N-aryl-5-azidomethyl- 2-oxazolidinone could provide access for rapid preparation of various oxazolidinone analogues.

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