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89791-57-1

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89791-57-1 Usage

Molecular Structure

The compound consists of a six-membered dioxane ring with two bromino atoms attached to one of the carbon atoms, and a 1,2-dibromoethyl group attached to another carbon atom.

Appearance

It is a colorless liquid at room temperature.

Solubility

The compound is insoluble in water but soluble in organic solvents.

Uses

It is commonly used in organic synthesis and as a reagent in chemical reactions. Its primary use is as an intermediate in the production of other organic chemicals, in the synthesis of pharmaceuticals and agrochemicals, and as a crosslinking agent in polymer chemistry.

Toxicity

It is important to handle this compound with care due to its toxic nature and potential environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 89791-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,9 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89791-57:
(7*8)+(6*9)+(5*7)+(4*9)+(3*1)+(2*5)+(1*7)=201
201 % 10 = 1
So 89791-57-1 is a valid CAS Registry Number.

89791-57-1SDS

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 2-(1,2-dibromoethyl)-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-(1,2-dibromoethyl)1,3-dioxane

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:89791-57-1 SDS

89791-57-1Downstream Products

89791-57-1Relevant articles and documents

Synthesis and Some Transformations of Cyclic Acetals of Propargyl Aldehyde

Lukicheva,Golovanov,Nachkebia, Ya. A.,Bekin,Raskildina,Zlotskii

, p. 330 - 333 (2018/03/26)

Dehydrobromination of 2-(1,2-dibromoethyl)-1,3-dioxocyclanes with sodium amide in liquid ammonia provided cyclic acetals of propargyl aldehyde. Reactions of the resulting compounds with nitrile oxides and diazomethane afforded the corresponding isoxazole and pyrazole derivatives.

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