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1,3-Dioxane, 4-methyl-2-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5702-50-1

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5702-50-1 Usage

Physical state

Colorless liquid

Odor

Faint, sweet

Classification

Volatile organic compound

Common uses

a. Solvent
b. Production of other chemicals
c. Manufacturing of paints
d. Manufacturing of adhesives
e. Manufacturing of cleaning products

Environmental and health concerns

a. Potential environmental hazard
b. Suspected carcinogen
c. Adverse effects on the nervous system

Efforts to limit use

a. Finding alternative, safer compounds
b. Reducing industrial applications
c. Promoting safer chemical usage

Check Digit Verification of cas no

The CAS Registry Mumber 5702-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5702-50:
(6*5)+(5*7)+(4*0)+(3*2)+(2*5)+(1*0)=81
81 % 10 = 1
So 5702-50-1 is a valid CAS Registry Number.

5702-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-isopropyl-4-methyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-Isopropyl-4-methyl-<1,3>dioxan

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:5702-50-1 SDS

5702-50-1Downstream Products

5702-50-1Relevant academic research and scientific papers

On the Mechanism of the Lewis Acid Mediated Cleavage of Chiral Acetals

Sammakia, Tarek,Smith, Randall S.

, p. 2997 - 3000 (2007/10/02)

The TiCl4-promoted cleavage of acetals has been shown to proceed by different mechanisms depending on the structure of the acetal, making it difficult to draw firm conclusions about the mechanism of related acetals based on model studies.

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