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132353-05-0

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132353-05-0 Usage

Physical state

Colorless liquid

Odor

Faint

Usage

Solvent in industrial processes
Production of adhesives
Production of sealants
Cleaning products

Additional uses

Stabilizer in plastic manufacturing
Component in some pharmaceuticals

Health concerns

Likely human carcinogen (according to the International Agency for Research on Cancer)

Safety precautions

Handle and store with caution
Use appropriate protective equipment when working with this substance

Check Digit Verification of cas no

The CAS Registry Mumber 132353-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,5 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132353-05:
(8*1)+(7*3)+(6*2)+(5*3)+(4*5)+(3*3)+(2*0)+(1*5)=90
90 % 10 = 0
So 132353-05-0 is a valid CAS Registry Number.

132353-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(benzenesulfonyl)ethyl]-1,4-dioxane

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:132353-05-0 SDS

132353-05-0Downstream Products

132353-05-0Relevant articles and documents

Addition to electron deficient olefins of α-oxy carbon-centered radicals, generated from cyclic ethers and acetals by the reaction with alkylperoxy- λ3-iodane

Sueda, Takuya,Takeuchi, Yasunori,Suefuji, Takashi,Ochiai, Masahito

, p. 195 - 200 (2007/10/03)

Thermal decomposition of 1-tert-butylperoxy-1,2-benziodoxol-3(1H)-one in cyclic ethers and acetals at 50°C generates α-oxy carbon-centered radicals, which undergo an addition reaction with vinyl sulfones and unsaturated esters.

N-HYDROXY-2-PYRIDINETHIONE: A MILD AND CONVENIENT SOURCE OF HYDROXYL RADICALS

Boivin, Jean,Crepon, Elisabeth,Zard, Samir Z.

, p. 6869 - 6872 (2007/10/02)

N-Hydroxy-2-thiopyridone gives hydroxyl radicals on irradiationm with visible light and these can be incorporated in useful radical chain processes involving hydrogen abstraction.

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