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

13297-07-9

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13297-07-9 Usage

Physical state

Clear, colorless liquid

Odor

Slightly sweet

Uses

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Derivative

Dioxane (commonly used as a solvent in laboratory and industrial processes)

Hazard classification

Hazardous substance

Health hazards

Causes skin and eye irritation, harmful if swallowed or inhaled

Importance

Important building block for the production of various important compounds in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 13297-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13297-07:
(7*1)+(6*3)+(5*2)+(4*9)+(3*7)+(2*0)+(1*7)=99
99 % 10 = 9
So 13297-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO2/c7-3-2-6-8-4-1-5-9-6/h6H,1-5H2

13297-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloroethyl)-1,3-dioxane

1.2 Other means of identification

Product number -
Other names EINECS 236-319-9

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:13297-07-9 SDS

13297-07-9Relevant academic research and scientific papers

LES ORGANOSILICIQUES COMME AGENTS DE SYNTHESE D'ACETALS β-HALOGENES

GIL, Gerard

, p. 3805 - 3808 (2007/10/02)

The reactions of unsaturated aldehydes and ketones with diols in presence of halogenosilane lead to the synthesis of halogenoacetals in yields of 60-97percent.

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