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2,5-Oxazolidinedione, 4-(1-bromoethyl)-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83791-33-7

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83791-33-7 Usage

Structure

2,5-oxazolidinedione ring with a 4-(1-bromoethyl)-4-methoxy substituent
The compound features a five-membered heterocyclic ring containing a bromine atom and a methoxy group.

Type

Heterocyclic compound
The 2,5-oxazolidinedione ring is a heterocyclic structure, meaning it contains atoms of different elements.

Application

Synthesis and production of pharmaceuticals and organic compounds
This chemical is used in the creation of various pharmaceuticals and organic compounds, making it valuable in the field of chemistry.

Potential

Medicinal chemistry and drug discovery
Due to its unique structure and reactivity, 2,5-Oxazolidinedione, 4-(1-bromoethyl)-4-methoxymay have significant applications in medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 83791-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83791-33:
(7*8)+(6*3)+(5*7)+(4*9)+(3*1)+(2*3)+(1*3)=157
157 % 10 = 7
So 83791-33-7 is a valid CAS Registry Number.

83791-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-Bromo-ethyl)-4-methoxy-oxazolidine-2,5-dione

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:83791-33-7 SDS

83791-33-7Relevant academic research and scientific papers

REACTION OF 4-BROMOALKYL-4-METHOXY-2,5-OXAZOLIDIONE WITH ALCOHOL OR α-AMINO ACID ESTER AND TRANSFORMATIONS OF THE PRODUCTS

Shin, Chung-gi,Takamatsu, Naoyuki,Sato, Yoshiaki,Yonezawa, Yasuchika

, p. 603 - 609 (2007/10/02)

Reaction of N-carboxy α-dehydroamino acid anhydride with methanol in the presence of NBS gave 4-bromoalkyl-4-methoxy-2,5-oxazolidone, which was further treated with alcohol or α-amino acid ester to give extremely different two types of products, 2-oxazoli

SYNTHESIS OF NEW 2-OXAZOLINONES FROM N-CARBOXY α-DEHYDROAMINO ACID ANHYDRIDES

Yonezawa, Yasuchika,Shin, Chung-gi,Ohtsu, Akira,Yoshimura, Juji

, p. 1171 - 1172 (2007/10/02)

Addition of methanol to N-carboxy α-dehydroamino acid anhydride in the presence of NBS, followed by the treatment of the resulting product with base gave a new 2-oxazolinone-4-carboxylate.

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