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.
55702-41-5Relevant 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.