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1-butyl-3-(4-methoxyphenyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26849-50-3

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26849-50-3 Usage

Chemical class

Urea derivative

Appearance

White or off-white crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Usage

a. Organic synthesis
b. Pharmaceutical research (building block for pharmacologically active compounds)

Potential applications

a. Agriculture (herbicide)
b. Therapeutic properties (antiproliferative and anticancer agent)

Versatility

Applications in various industries and scientific research fields

Check Digit Verification of cas no

The CAS Registry Mumber 26849-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26849-50:
(7*2)+(6*6)+(5*8)+(4*4)+(3*9)+(2*5)+(1*0)=143
143 % 10 = 3
So 26849-50-3 is a valid CAS Registry Number.

26849-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-3-(4-methoxyphenyl)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:26849-50-3 SDS

26849-50-3Downstream Products

26849-50-3Relevant academic research and scientific papers

Lanthanum(III) Trifluoromethanesulfonate Catalyzed Direct Synthesis of Ureas from N-Benzyloxycarbonyl-, N -Allyloxycarbonyl-, and N -2,2,2-Trichloroethoxycarbonyl-Protected Amines

Bui, Tien Tan,Kim, Hee-Kwon

supporting information, p. 997 - 1002 (2020/06/17)

A novel lanthanum triflate mediated conversion of N -benzyloxycarbonyl-, N -allyloxycarbonyl-, and N -trichloroethoxycarbonyl-protected amines into nonsymmetric ureas was discovered. In this study, lanthanum triflate was found to be an effective catalyst for preparing various nonsymmetric ureas from protected amines. A variety of protected aromatic and aliphatic carbamates reacted readily with various amines in the presence of lanthanum triflate to generate the desired ureas in high yields. This result demonstrated that this novel lanthanum triflate catalyzed preparation of ureas from Cbz, Alloc, and Troc carbamates can be employed for the formation of various urea structures.

Dynamic Ureas with Fast and pH-Independent Hydrolytic Kinetics

Cai, Kaimin,Ying, Hanze,Cheng, Jianjun

supporting information, p. 7345 - 7348 (2018/06/11)

Low cost, high performance hydrolysable polymers are of great importance in biomedical applications and materials industries. While many applications require materials to have a degradation profile insensitive to external pH to achieve consistent release profiles under varying conditions, hydrolysable chemistry techniques developed so far have pH-dependent hydrolytic kinetics. This work reports the design and synthesis of a new type of hydrolysable polymer that has identical hydrolysis kinetics from pH 3 to 11. The unprecedented pH independent hydrolytic kinetics of the aryl ureas were shown to be related to the dynamic bond dissociation controlled hydrolysis mechanism; the resulting hindered poly(aryl urea) can be degraded with a hydrolysis half-life of 10 min in solution. More importantly, these fast degradable hindered aromatic polyureas can be easily prepared by addition polymerization from commercially available monomers and are resistant to hydrolysis in solid form for months under ambient storage conditions. The combined features of good stability in solid state and fast hydrolysis at various pH values is unprecedented in polyurea material, and will have implications for materials design and applications, such as sacrificial coatings and biomaterials.

KINETICS OF REACTIONS OF para-SUBSTITUTED PHENYL ISOCYANATES WITH AMINES AND ALCOHOLS

Danihel, Ivan,Barnikol, Falk,Kristian, Pavol

, p. 1662 - 1670 (2007/10/02)

The reaction of para-substituted phenyl isocyanates with amines and alcohols was studied by stopped-flow method.The Hammett correlation obtained showed that the sensitivity of the above mentioned reactions toward substituent effects is the same as that of

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