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71363-52-5

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71363-52-5 Usage

Uses

Dimethylvinphos is a moderately persistent insecticide with contact and stomach action and is used to control stem borers and leaf rollers in rice with a dust formulation.

Metabolism

The main degradation route in mammals is O-demethylation to desmethyl dimethylvinphos, which is hydrolyzed to 2,2,4- trichloroacetophenone.

Toxicity evaluation

The acute oral LD50 for rats is 155–210 mg/kg. Inhalation LC50 (4 h) for male and female rats is 970–1189 and >4900 mg/m3 air.

Check Digit Verification of cas no

The CAS Registry Mumber 71363-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,6 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71363-52:
(7*7)+(6*1)+(5*3)+(4*6)+(3*3)+(2*5)+(1*2)=115
115 % 10 = 5
So 71363-52-5 is a valid CAS Registry Number.

71363-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(2,4-dichlorophenyl)vinyldimethyl phosphate

1.2 Other means of identification

Product number -
Other names DIMETHYLVINPHOS

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:71363-52-5 SDS

71363-52-5Downstream Products

71363-52-5Relevant articles and documents

REACTIONS OF 2,4- AND 2,6-DICHLOROPHENACYLIDENE HALIDES WITH TRIALKYLPHOSPHITES IN PROTIC SOLVENTS. DIRECT EVIDENCE FOR THE "ENOLATE ANION" PATHWAY

Mlotkowska, Barbara,Majewski, Piotr,Koziara, Anna,Zwierzak, Andrzej,Sledzinski, Bohdan

, p. 631 - 642 (2007/10/02)

The reactions of 2,6-dichlorophenacyl and 2,6-dichlorophenacylidene chlorides and bromides with trimethyl and triethyl phosphites have been investigated.The reactivity of 2,6-dichlorophenacylidene chloride and bromide towards trialkyl phosphites was compared with that of 2,4-dichlorophenacylidene chloride and bromide.The influence of methanol, acting as a model protic solvent, on the above mentioned processes has also benn investigated.The mechanism of Perkow reaction of sterically hindered α-haloketones with bulky substituents around the carbonyl center is discussed.

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