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4-Vinyl-1,3-dioxane is a colorless liquid chemical compound with the molecular formula C5H8O2. It is an organic compound that features a vinyl group (C=C) attached to a 1,3-dioxane ring, which consists of two oxygen atoms and three carbon atoms. 4-vinyl-1,3-dioxane is primarily used as a monomer in the production of polymers and copolymers, particularly in the synthesis of polyethers and polyurethanes. Due to its reactive vinyl group, 4-vinyl-1,3-dioxane can undergo various polymerization reactions, making it a valuable intermediate in the chemical industry. It is also known for its low toxicity and high solubility in water, which further enhances its utility in various applications.

1072-96-4

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1072-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072-96-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1072-96:
(6*1)+(5*0)+(4*7)+(3*2)+(2*9)+(1*6)=64
64 % 10 = 4
So 1072-96-4 is a valid CAS Registry Number.

1072-96-4SDS

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 4-ethenyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 6-vinyl-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:1072-96-4 SDS

1072-96-4Downstream Products

1072-96-4Relevant academic research and scientific papers

Ruthenium-catalysed Prins Reaction

Thivolle-Cazat, Jean,Tkatchenko, Igor

, p. 1128 - 1129 (2007/10/02)

The reactions of dienes and alkenes with aldehydes and carboxylic acids leading to derivatives of 1,3-diols are catalysed by ruthenium salts under mild conditions; oxygenated compounds of higher molecular weight may also be produced by variations in the reaction conditions.

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