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Urea, N-butyl-N'-(2,4-dimethylphenyl)-N-(phenylmethyl)-, also known as a substituted urea, is a chemical compound that serves as a versatile intermediate in the synthesis of various organic compounds. It is characterized by its colorless to pale yellow liquid appearance and a faint odor. Due to its reactivity with strong acids, bases, and oxidizing agents, it requires careful handling and adherence to safety protocols to mitigate potential hazards.

88451-06-3

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88451-06-3 Usage

Uses

Used in Pesticide Production:
Urea, N-butyl-N'-(2,4-dimethylphenyl)-N-(phenylmethyl)is used as a key raw material in the production of pesticides. Its chemical structure allows for the development of active ingredients that can effectively control and manage pests, thereby protecting crops and enhancing agricultural productivity.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Urea, N-butyl-N'-(2,4-dimethylphenyl)-N-(phenylmethyl)- is utilized as an intermediate for the synthesis of various drugs. Its unique structure contributes to the development of pharmaceuticals with specific therapeutic properties, addressing a range of health conditions.
Used in Herbicide Formulation:
Urea, N-butyl-N'-(2,4-dimethylphenyl)-N-(phenylmethyl)is employed as an intermediate in the formulation of herbicides. Its incorporation aids in the creation of herbicidal agents that target and control the growth of unwanted plants, thus improving crop yield and quality.
Used in Fungicide Development:
This chemical compound is also used in the development of fungicides, playing a crucial role as an intermediate in their synthesis. Its contribution to the formulation of fungicides helps in combating fungal infections that can damage crops and reduce agricultural output.
Used in Plant Growth Regulator Production:
Urea, N-butyl-N'-(2,4-dimethylphenyl)-N-(phenylmethyl)is utilized in the production of plant growth regulators, which are essential for managing and optimizing plant growth. Its role as an intermediate allows for the development of regulators that can enhance crop growth and improve resistance to various environmental stresses.

Check Digit Verification of cas no

The CAS Registry Mumber 88451-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88451-06:
(7*8)+(6*8)+(5*4)+(4*5)+(3*1)+(2*0)+(1*6)=153
153 % 10 = 3
So 88451-06-3 is a valid CAS Registry Number.

88451-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1-butyl-3-(2,4-dimethylphenyl)urea

1.2 Other means of identification

Product number -
Other names -

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:88451-06-3 SDS

88451-06-3Relevant academic research and scientific papers

Potential Antiatherosclerotic Agents. 6. Hypocholesterolemic Trisubstituted Urea Analogues

DeVries, Vern G.,Bloom, Jonathan D.,Dutia, Minu D.,Katocs, Andrew S.,Largis, Elwood E.

, p. 2318 - 2325 (2007/10/02)

The discovery that a series of N,N-dialkyl-N'-arylureas were inhibitors of the ACAT enzyme has led to a structure-activity study involving the systematic modification of three sites of the urea backbone.This study culminated in the selection of N'-(2,4-dimethylphenyl)-N-benzyl-N-n-butylurea (115) for more extensive biological evaluation.ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.

Antiatherosclerotic ureas and thioureas

-

, (2008/06/13)

This invention is concerned with ureas and thioureas which may be represented by the formula: STR1 wherein X represents at least one substituent selected from the group consisting of (C1 -C4)alkyl, (C1 -C4)alken

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