Welcome to LookChem.com Sign In|Join Free
  • or
4-(2,2-Dichlorovinyl)phenol, also known as DCP, is a synthetic chemical compound that is a derivative of phenol. It is classified as a chlorinated aromatic compound and is widely used as an intermediate in the production of various chemicals, such as herbicides, insecticides, and fungicides. DCP is known to have toxicological effects on the environment and human health, with potential carcinogenic, mutagenic, and teratogenic properties. It is also a persistent organic pollutant and has been listed as a priority substance under the European Water Framework Directive. Due to its hazardous properties, there are strict regulations and guidelines for its handling, use, and disposal.

83671-20-9

Post Buying Request

83671-20-9 Suppliers

Recommended suppliers

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

83671-20-9 Usage

Uses

Used in Chemical Production Industry:
4-(2,2-Dichlorovinyl)phenol is used as an intermediate for the production of various chemicals, such as herbicides, insecticides, and fungicides, due to its reactivity and versatility in chemical synthesis.
Used in Environmental Management:
4-(2,2-Dichlorovinyl)phenol is used as a priority substance for monitoring and regulation under the European Water Framework Directive, as it is a persistent organic pollutant with potential toxicological effects on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 83671-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83671-20:
(7*8)+(6*3)+(5*6)+(4*7)+(3*1)+(2*2)+(1*0)=139
139 % 10 = 9
So 83671-20-9 is a valid CAS Registry Number.

83671-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2-dichloroethenyl)-4-hydroxybenzene

1.2 Other means of identification

Product number -
Other names p-hydroxy-

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:83671-20-9 SDS

83671-20-9Downstream Products

83671-20-9Relevant academic research and scientific papers

METHOXYIMINO COMPOUNDS AND FUNGICIDE COMPOSITION COMPRISING SAME

-

Page/Page column 17-18, (2009/07/17)

The present invention provides a methoxyimino compound, and a fungicide composition comprising same as an active ingredient. The methoxyimino compound of the present invention, which has an excellent antifungal activity against a wide spectrum of fungi even at a low application rate, can be used to protect various crops.

SmI2-mediated elimination reaction of trichloromethyl carbinols: A facile method to synthesize vinyl dichlorides

Li, Jian,Xu, Xiaoliang,Zhang, Yongmin

, p. 9349 - 9351 (2007/10/03)

Samarium diiodide-mediated elimination reaction provides a simple and general method to synthesize vinyl dichlorides from trichloromethyl carbinols directly in good to excellent yields.

Conversion of aromatic aldehydes into 1-aryl-2,2-dichloroethenes

Nenajdenko,Shastin,Korotchenko,Balenkova

, p. 1047 - 1050 (2007/10/03)

A new general one-pot preparative method for the synthesis of 1-aryl(hetaryl)-2,2-dichloroethenes from aldehydes was developed. The method involves successive conversions of the latter into hydrazones followed by treatment with carbon tetrachloride in the

Reductive Addition of Polyhalomethanes and Their Related Compounds to Aldehydes and 1,2-Elimination of the Coupling Products in a Pb/Al Bimetal Redox System

Tanaka, Hideo,Yamashita, Shiro,Yamanoue, Motoi,Torii, Sigeru

, p. 444 - 450 (2007/10/02)

A Pb/Al bimetal system was used to carry out reductive addition of tetrachloromethane, tetrabromomethane, bromotrichloromethane, trichloroacetamide, and trichloroacetonitrile to aldehydes.Subsequent 1,2-elimination of the halogen atom and hydroxyl group from the coupling products was also performed with the Pb/Al bimetal system.The technology was successfully applied to stereocontrolled syntheses of ethyl trans- and cis-3-(2,2-dihaloethenyl)-2,2-dimethylcyclopropanecarboxylates.

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 83671-20-9