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2617-72-3

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2617-72-3 Usage

Chemical class

Phenylurea

Function

Herbicide

Urea derivative

Yes

Chlorinated phenyl rings

Two

Chlorine atoms

Four

Effectiveness

Inhibits growth of weeds and undesirable vegetation

Environmental impact

Can be harmful if not properly managed

Safety precautions

Handle with caution

Application

Control of unwanted plant growth

Check Digit Verification of cas no

The CAS Registry Mumber 2617-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2617-72:
(6*2)+(5*6)+(4*1)+(3*7)+(2*7)+(1*2)=83
83 % 10 = 3
So 2617-72-3 is a valid CAS Registry Number.

2617-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-3-(3,4-dichlorophenyl)urea

1.2 Other means of identification

Product number -
Other names 3,3',4-trichlorocarbanilide

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:2617-72-3 SDS

2617-72-3Downstream Products

2617-72-3Relevant articles and documents

Antischistosomal activity of N,N′-arylurea analogs against Schistosoma japonicum

Yao, Houzong,Liu, Fengyou,Chen, Jinglei,Li, Yan,Cui, Jinhao,Qiao, Chunhua

supporting information, p. 1386 - 1390 (2016/02/19)

Although the antischistosomal activities of N,N′-arylurea analogs were reported, systematic structure-activity relationships have not been conducted. In this Letter, we reported the design, synthesis and evaluation of 45 N,N′-arylurea analogs. Among these prepared compounds, 13 compounds were urea linker modified and 32 were N,N′-arylurea derivatives. The activity evaluation revealed 12 analogs exhibited IC50 values lower than 22.6 μM, and 7 of them had IC50 less than 10 μM against the juvenile Schistosoma japonicum in vitro. Their worm killing potency was even higher against adult worm. Unfortunately, low to moderate worm burden reduction of 0-33.4% was recorded after administration of a single oral dose of 200 mg/kg or 400 mg/kg to mice harboring S. japonicum.

Compositions

-

, (2008/06/13)

The problem of providing a storage stable anti-calculus toothpaste comprising a tripolyphosphate salt is remedied by incorporating more than 4% of the salt and having the pH from about 8 to about 10. A tripolyphosphate salt may also be combined with a noncationic anti-bacterial agent such as triclosan to provide a composition having anti-calculus and anti-plaque activity.

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