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Phenyl, 3-chloro-, also known as 3-Chlorotoluene, is an organic compound with the chemical formula C7H7Cl. It is a colorless liquid with a strong, aromatic odor and is derived from toluene by substituting one hydrogen atom with a chlorine atom at the third carbon position. This halogenated aromatic compound is used as an intermediate in the production of various chemicals, such as dyes, pharmaceuticals, and agrochemicals. Due to its reactivity and potential health risks, it is essential to handle 3-Chlorotoluene with proper safety measures and precautions.

3474-40-6

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3474-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3474-40-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3474-40:
(6*3)+(5*4)+(4*7)+(3*4)+(2*4)+(1*0)=86
86 % 10 = 6
So 3474-40-6 is a valid CAS Registry Number.

3474-40-6SDS

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 m-Chlorophenyl radical

1.2 Other means of identification

Product number -
Other names m-Chlor-phenyl-Radikal

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:3474-40-6 SDS

3474-40-6Downstream Products

3474-40-6Relevant academic research and scientific papers

Magnetic Field Effects on the Photodissociation Reaction of Triarylphosphine in Nonviscous Homogeneous Solutions

Sakaguchi, Yoshio,Hayashi, Hisaharu

, p. 3421 - 3429 (2004)

The magnetic field effects (MFEs) on the photodecomposition reactions of triphenylphosphine and its halogen and methyl derivatives are investigated in fluid solutions. The yield of diarylphosphinyl radicals decreased with increasing magnetic field from 0.1 to 5 T but was stationary below 0.1 T and above 5 T. The MFE becomes larger by the substitution of halogen atoms and the 3- or 4-methyl group. In cyclohexane, the yields of the escaped diarylphosphinyl radicals at 1 T are reduced to 0.69, 0.55, 0.59, and 0.56 of those at 0 T for triphenylphosphine and its tris(4-chloro), tris(3-methyl), and tris(4-methyl) derivatives, respectively. This magnetic field dependence was ascribed to originate from the deactivation process of the excited triplet state, which is a variant of the d-type triplet mechanism originally proposed by Steiner. The interaction between the closely lying nπ* and ππ* states makes their solvent dependence complicated.

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