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60096-27-7

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60096-27-7 Usage

Structure

Benzene derivative with a selenium atom in the benzene ring

Appearance

White to light yellow solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Building block in organic synthesis, potential applications in pharmaceutical and materials industries

Chelating agent

Potential due to the presence of selenium

Antioxidant and anticancer properties

Has been studied for these potential properties

Safety

Careful handling and proper lab safety procedures should be followed when working with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 60096-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,9 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60096-27:
(7*6)+(6*0)+(5*0)+(4*9)+(3*6)+(2*2)+(1*7)=107
107 % 10 = 7
So 60096-27-7 is a valid CAS Registry Number.

60096-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-3H-1-benzoselenophene

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-2,3-dihydrobenzo[b]selenophene

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:60096-27-7 SDS

60096-27-7Relevant articles and documents

Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides

Stefani, Helio A.,Petragnani, Nicola,Ascenso, Maria F. C.,Zeni, Gilson

, p. 2161 - 2166 (2007/10/03)

Selenofuran derivatives were prepared using several phenyl alkenyl selenides via seleno-Claisen rearrangement.

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