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74925-48-7

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74925-48-7 Usage

Molecular Structure

Contains a 1H-indene ring with two chlorine atoms attached at positions 1 and 2, and a hydrogen atom at position 3.

Physical State

Colorless liquid.

Uses

Mainly used as an intermediate in the production of various compounds, including pharmaceuticals, agrochemicals, and polymers. Utilized in the synthesis of organic chemicals and as a solvent for chemical reactions. Potential applications in material science and as a building block for specialty chemicals.

Importance

Versatile reactivity and usefulness in various industrial processes make it an important compound with a wide range of potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 74925-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,2 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74925-48:
(7*7)+(6*4)+(5*9)+(4*2)+(3*5)+(2*4)+(1*8)=157
157 % 10 = 7
So 74925-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Cl2/c10-8-5-6-3-1-2-4-7(6)9(8)11/h1-4,8-9H,5H2

74925-48-7SDS

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 1,2-dichloro-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 1,2-Dichloroindane

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:74925-48-7 SDS

74925-48-7Relevant articles and documents

Organocatalytic, Enantioselective Dichlorination of Unfunctionalized Alkenes

Wedek, Volker,Van Lommel, Ruben,Daniliuc, Constantin G.,De Proft, Frank,Hennecke, Ulrich

supporting information, p. 9239 - 9243 (2019/07/16)

The use of a new class of unsymmetrical cinchona-alkaloid-based, phthalazine-bridged organocatalysts enabled the highly enantioselective dichlorination of unfunctionalized alkenes. In combination with the electrophilic chlorinating agent 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) and triethylsilyl chloride (TES-Cl) as the source of nucleophilic chloride, 1-aryl-2-alkyl alkenes were dichlorinated with enantioselectivities of up to 94:6 er. Initial mechanistic investigations suggest that no free chlorine is formed, and by replacement of the chloride by fluoride, enantioselective chlorofluorinations of alkenes are possible.

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