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1-((2-CHLOROPHENYL)METHYL)-3-(4-METHYLPHENYL)UREA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138111-35-0

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138111-35-0 Usage

Chemical Class

Phenylureas

Use

Herbicide

Target

Grasses in crops

Crop Applications

Soybeans, peanuts, cotton

Mechanism of Action

Inhibits growth of grasses

Selectivity

Selective herbicide

Mammalian Toxicity

Low toxicity to mammals

Environmental Impact

Low environmental impact when used according to label instructions

Safety Precautions

Handle with care and follow safety guidelines to avoid potential risks

Check Digit Verification of cas no

The CAS Registry Mumber 138111-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,1 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138111-35:
(8*1)+(7*3)+(6*8)+(5*1)+(4*1)+(3*1)+(2*3)+(1*5)=100
100 % 10 = 0
So 138111-35-0 is a valid CAS Registry Number.

138111-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-chlorophenyl)methyl]-3-(4-methylphenyl)urea

1.2 Other means of identification

Product number -
Other names Urea,N-[(2-chlorophenyl)methyl]-N'-(4-methylphenyl)

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:138111-35-0 SDS

138111-35-0Downstream Products

138111-35-0Relevant academic research and scientific papers

A high-yielding, expeditious, and multicomponent synthesis of urea and carbamate derivatives by using triphenylphosphine/trichloroisocyanuric acid system

Ghodsinia, Sara S.E.,Akhlaghinia, Batool

, p. 104 - 110 (2016)

An efficient method for the synthesis of urea and carbamate derivatives from amines and alcohols is described by using triphenylphosphine (PPh3)/trichloroisocyanuric acid system. The protocol allows for the preparation of symmetrical, unsymmetrical di, tri-, and tetra-substituted ureas and carbamates and is tolerant of a wide range of functional groups. To optimize the reaction conditions, experimental variables including temperature, the concentration of amine and alcohol, solvent, and reaction time were studied. Satisfactory yields were obtained at the optimized conditions. The present methodology is experimentally simple, mild, and represents a valuable alternative to the existing methods.

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