Welcome to LookChem.com Sign In|Join Free
  • or
"Benzene, 1,1'-(2,2-dichlorocyclopropylidene)bis-" is a chemical compound with the molecular formula C9H10Cl4. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. Benzene, 1,1'-(2,2-dichlorocyclopropylidene)bis- is primarily used as an insecticide, specifically for the control of termites and other wood-destroying organisms. It is also known as "Dichlofenthion" or "Bis(2,2-dichlorocyclopropyl) ether." Due to its toxicity and potential environmental impact, its use is regulated in many countries. The compound is characterized by its ability to disrupt the nervous system of insects, leading to paralysis and death. It is important to handle this chemical with care due to its potential hazards to human health and the environment.

3141-42-2

Post Buying Request

3141-42-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3141-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3141-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3141-42:
(6*3)+(5*1)+(4*4)+(3*1)+(2*4)+(1*2)=52
52 % 10 = 2
So 3141-42-2 is a valid CAS Registry Number.

3141-42-2SDS

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 (2,2-dichloro-1-phenylcyclopropyl)benzene

1.2 Other means of identification

Product number -
Other names 2,2-Dichlor-1,1-diphenyl-cyclopropan

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:3141-42-2 SDS

3141-42-2Relevant academic research and scientific papers

Arylcyclopropane Photochemistry. Effects of Electron-Donating and Electron-Withdrawing Aromatic Substituents on the Photochemical Rearrangements of 1,1-Diarylcyclopropanes.

Hixson, Stephen S.,Franke, Lothar A.

, p. 2706 - 2711 (2007/10/02)

Irradiation of 1,1-diarylcyclopropanes 4a-g, having substituents X and Y at the para positions of the aromatic rings, afforded 1,1-diarylpropenes 5a-g and 1-arylindans 6a-f.The rate constants of these (singlet state) reactions, determined from the reactan

Carbon Tetrachloride-Dimethyl Sulphone-Potassium Hydroxide-t-Butyl Alcohol: a Convenient New Reagent for gem-Dichloromethylenation of Alkenes

Poon, Chi-Duen,Yuen, Po-Wai,Man, Tim-On,Li, Chun-Sing,Chan, Tze-Lock

, p. 1561 - 1563 (2007/10/02)

The action of dimethyl sulphone-potassium hydroxide-t-butyl alcohol on carbon tetrachloride readily affords dichlorocarbene.In the presence of alkenes, gem-dichlorocyclopropanes are formed in moderate to high yields.The dichlorocarbene generated by this procedure adds stereospecifically to alkenes with retention of geometric configuration about the carbon-carbon double bond.Relative reactivities of alkenes towards the CCl4-derived dichlorocarbene parallel the nucleophilicities of the alkenes and indicate that free dichlorocarbene is probably involved.

REACTIONS OF CARBENES WITH DIENE AND POLYENE COMPOUNDS. XI. REACTION OF DICHLOROCARBENE WITH ALLENE HYDROCARBONS

Kostikov, R. R.,Vorob'eva, I. S.,Molchanov, A. P.

, p. 229 - 234 (2007/10/02)

The addition of dichlorocarbene to 1-phenyl-1,2-alkadienes takes place regioselectively at the most substituted multiple bond.On heating, the initial reaction products isomerize to the corresponding (dichloromethylene)cyclopropanes.

THERMAL TRANSFORMATIONS OF GEM-DIHALOGENODIPHENYLCYCLOPROPANES

Kostikov, R. R.,Varakin, G. S.,Ogloblin, K. A.

, p. 1438 - 1444 (2007/10/02)

When gem-dihalogenodiphenylcyclopropanes are heated, 2-halogenophenylindenes or diphenyl-2-halogeno-1,3-alkadienes are formed.The yields of the substituted indenes are increased in the presence of acidic catalysts, while the yield of the dienes is increas

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3141-42-2