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112233-59-7

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112233-59-7 Usage

Molecular structure

Consists of a cyclohexene ring, a trichloromethylthio group, and a hydroxy group.

Classification

Isoindolone derivative.

Usage

Employed in the field of organic synthesis.

Potential applications

May have uses in pharmaceuticals, agrochemicals, and materials science.

Research and testing

Further studies are needed to understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 112233-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112233-59:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*3)+(2*5)+(1*9)=77
77 % 10 = 7
So 112233-59-7 is a valid CAS Registry Number.

112233-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclohex-2-enyl-3-hydroxy-2-trichloromethylsulfanyl-2,3-dihydro-isoindol-1-one

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:112233-59-7 SDS

112233-59-7Downstream Products

112233-59-7Relevant articles and documents

PHOTOINDUCED PARA-CYCLOADDITION OF PHTHALIMIDES

Schwack, Wolfgang

, p. 1869 - 1872 (1987)

N-Substituted phthalimides (R= -SCCl3, -CH3, phenyl) reacted with cyclohexene on irradiation at λ> 280 nm by way of para-cycloaddition, yielding N-substituted tricyclo(4.2.2.0)dodeca-8,11-diene-9,10-dicarboximides.The N-(trichloromethylthio)phthalimide gave the cycloadduct as by-product, while for N-methyl- and N-phenylphthalimide the para-cycloaddition predominated.

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