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4405-42-9

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4405-42-9 Usage

Functional groups

Chloro-substituted aromatic compound, trimethylsilyl group

Structure

Benzene ring with a chlorine atom at the 3-position and a trimethylsilyl group at the 1-position

Applications

Organic synthesis, pharmaceutical and agricultural industries, specialty chemicals and materials

Reactivity

Can undergo cross-coupling and halogenation reactions

Protective group

Trimethylsilyl group allows for selective reactions at other functional groups

Versatility

Presence of both chloro and trimethylsilyl groups makes the compound useful for synthetic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 4405-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4405-42:
(6*4)+(5*4)+(4*0)+(3*5)+(2*4)+(1*2)=69
69 % 10 = 9
So 4405-42-9 is a valid CAS Registry Number.

4405-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Trimethylsilyl)-3-chlorobenzene

1.2 Other means of identification

Product number -
Other names Silane, (3-chlorophenyl)trimethyl-

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:4405-42-9 SDS

4405-42-9Relevant articles and documents

Halogen/lithium exchange in hydrocarbon media; Basic and continuous reactor studies

Slocum,Kusmic, Damir,Raber, Jeffrey C.,Reinscheld, Thomas K.,Whitley, Paul E.

body text, p. 4793 - 4796 (2010/10/02)

The halogen/lithium (X/Li) exchange's usefulness is challenged by the extreme conditions employed during the conversion of a bromo or an iodo substituent to an organolithium intermediate. Our preliminary disclosure reveals that simple X/Li exchanges can be accomplished at ambient temperature and in doped hydrocarbon media using n-BuLi. Use of a continuous reactor featuring brief reaction times (≤1 s) and large product throughputs further facilitates the production of a product resulting from a sequential X/Li exchange and nucleophilic addition.

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