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Urea, 3, 3-p-phenylenebis[1-phenyl-2-thiois a complex organic compound that consists of urea and 3,3-p-phenylenebis[1-phenyl-2-thio-. Urea, an organic compound, is widely used in fertilizers and skincare products due to its ability to promote plant growth and moisturize the skin. On the other hand, 3,3-p-phenylenebis[1-phenyl-2-thiois a thioether compound that holds potential in organic synthesis and materials science. The combination of these two compounds results in a unique molecule with a variety of potential applications across different industries.

6279-49-8

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6279-49-8 Usage

Uses

Used in Agriculture:
Urea, 3, 3-p-phenylenebis[1-phenyl-2-thiois used as a fertilizer additive for enhancing plant growth. The presence of urea provides essential nitrogen, a vital nutrient for plants, while the 3,3-p-phenylenebis[1-phenyl-2-thiocomponent may offer additional benefits such as improved nutrient uptake or soil health.
Used in Cosmetics:
In the cosmetics industry, Urea, 3, 3-p-phenylenebis[1-phenyl-2-thiois used as a moisturizing agent in skincare products. The urea component helps to retain moisture in the skin, providing hydration and improving skin texture. The 3,3-p-phenylenebis[1-phenyl-2-thiomay contribute to the product's stability or offer additional skin benefits.
Used in Pharmaceutical Industry:
Urea, 3, 3-p-phenylenebis[1-phenyl-2-thiois used as an active pharmaceutical ingredient or an intermediate in the synthesis of drugs. The unique structure of Urea, 3, 3-p-phenylenebis[1-phenyl-2-thio- may provide specific therapeutic effects or improve the delivery and bioavailability of other drug molecules.
Used in Materials Science:
In materials science, Urea, 3, 3-p-phenylenebis[1-phenyl-2-thiois used in the development of new materials with specific properties. The thioether component may contribute to the formation of novel polymers, coatings, or other materials with unique characteristics.
Further research and experimentation are necessary to fully explore the potential uses and properties of Urea, 3, 3-p-phenylenebis[1-phenyl-2-thio-. Its complex structure and the combination of urea and thioether functionalities open up possibilities for innovative applications across various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 6279-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6279-49:
(6*6)+(5*2)+(4*7)+(3*9)+(2*4)+(1*9)=118
118 % 10 = 8
So 6279-49-8 is a valid CAS Registry Number.

6279-49-8SDS

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 1-phenyl-3-[4-(phenylcarbamothioylamino)phenyl]thiourea

1.2 Other means of identification

Product number -
Other names WLN: SUYMR&AC1LJXR3

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:6279-49-8 SDS

6279-49-8Relevant academic research and scientific papers

A facile synthesis of p-Bis(4-thiazolidinon-3-yl)phenylenes and related systems and related systems

Abdel-Megid,Awas

, p. 161 - 168 (2002)

p-Bis(4-thiazolidinon-3-yl)phenylenes were synthesized from cycloaddition of thioglycollic acid with schiff bases of p-phenylenediamine or by treatment of p-bis(thiouredo)phenylenes with ethyl chloroacetate. The effect of hydrazines, hydroxylamine, acetam

Unsymmetrically N,N′-Disubstituted Diarylthioureas and Their Coordination Compounds with Cu(II) and Ni(II)

Cheresova,Zhukova,Tatarintseva,Cheresov,Mukmeneva

, p. 1271 - 1275 (2007/10/03)

Some new unsymmetrically N,N′-disubstituted diarylthioureas were prepared, and their reactions of complex formation in solutions were studied. Coordination compounds of the synthesized thioureas with 3d metals(2+) (Cu, Ni) were isolated and shown to have a chelate structure of the general formula M(SN)2.

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