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55702-41-5

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55702-41-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is derived from benzene, which is a hydrocarbon with a six-carbon ring structure.

Explanation

The compound has two chlorine atoms attached to the benzene rings.

Explanation

A methoxymethylene group (-O-CH2-) is present in the compound, connecting the two benzene rings.

Explanation

The compound is used in the production of various industrial products, including dyes, pigments, and pharmaceuticals.

Explanation

It serves as a chemical intermediate in the synthesis of other organic compounds.

Explanation

The compound poses health risks if ingested or inhaled, and proper precautions should be taken when handling it.

Explanation

Due to its potential health and environmental hazards, it is crucial to follow safety guidelines and regulations when working with this compound.

Derivative of benzene

Yes

Contains chlorine atoms

Two

Contains methoxymethylene group

Yes

Industrial applications

Dyes, pigments, pharmaceuticals

Chemical intermediate

Yes

Toxicity

Toxic if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 55702-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,0 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55702-41:
(7*5)+(6*5)+(5*7)+(4*0)+(3*2)+(2*4)+(1*1)=115
115 % 10 = 5
So 55702-41-5 is a valid CAS Registry Number.

55702-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-[(4-chlorophenyl)-methoxymethyl]benzene

1.2 Other means of identification

Product number -
Other names Methyl-[bis-(4-chlor-phenyl)-methyl]-aether

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:55702-41-5 SDS

55702-41-5Downstream Products

55702-41-5Relevant articles and documents

Analysis of non-extractable DDT-related compounds in riverine sediments of the Teltow Canal, Berlin, by pyrolysis and thermochemolysis

Kronimus, Alexander,Schwarzbauer, Jan,Ricking, Mathias

, p. 5882 - 5890 (2006)

Eighteen pre-extracted samples derived from a subaquatic riverine sediment core taken from the Teltow Canal, Berlin (Germany), were treated by off-line TMAH-thermochemolysis and subsequently analyzed by GC-MS to investigate release and thermodegradation o

The Absolute Kinetics of Several Reactions of Substituted Diphenylcarbenes

Hadel, L. M.,Maloney, V. M.,Platz, M. S.,McGimpsey, W. G.,Scaiano, J. C.

, p. 2488 - 2491 (2007/10/02)

4,4'-dibromo-, 4-bromo-, 4,4'-dichloro-, 4-chloro-, 4-methyl-, 4,4'-dimethyl-, 4-phenyl-, 4-carbomethoxyl-, 4-cyano-, 4-cyano-4'-methyl-, and 4,4'-dimethyldiphenyldiazomethane were studied by laser flash photolysis.Excitation of the diazo compounds at 308 nm produced the corresponding diarylcarbenes.The kinetics of the reaction of the substituted carbenes with alkanes and methanol were examined.Hydrogen abstraction rates are largely insensitive to ring substitution, while the methanol reaction is accelerated considerably by p-methyl substitution and retarded by a para electron-withdrawing substituent.

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