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Urea, N-phenyl-N'-2-pyrimidinyl, also known as phenylpyrimidourea or PPU, is an organic compound with the chemical formula C12H11N3O. It is a derivative of urea, where one hydrogen atom is replaced by a phenyl group and another by a 2-pyrimidinyl group. Urea, N-phenyl-N'-2-pyrimidinyl- is a white crystalline solid and is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure and properties make it a versatile building block for the development of new compounds with potential applications in medicine and agriculture.

24386-29-6

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24386-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24386-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24386-29:
(7*2)+(6*4)+(5*3)+(4*8)+(3*6)+(2*2)+(1*9)=116
116 % 10 = 6
So 24386-29-6 is a valid CAS Registry Number.

24386-29-6SDS

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-pyrimidin-2-ylurea

1.2 Other means of identification

Product number -
Other names 1-PHENYL-3-PYRIMIDIN-2-YL-UREA

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:24386-29-6 SDS

24386-29-6Downstream Products

24386-29-6Relevant academic research and scientific papers

MOLECULAR CONFORMATION OF 1,3-PYRIDYLPHENYLUREAS BY 1H AND 13C NMR STUDY

Sudha, L. V.,Sathyanarayana, D. N.

, p. 141 - 146 (1985)

1H and 13C NMR spectra are reported for several 1,3-pyridylphenyl ureas.Analysis of the spectra yielded the chemical shifts.The variations in the chemical shifts have been discussed in terms of the molecular conformations.

Synthesis of new unsymmetrical 4,5-dihydroxy-2-imidazolidinones. Dynamic NMR spectroscopic study of the prototropic tautomerism in 1-(2-benzimidazolyl)- 3-phenyl-4,5-dihydroxy-2-imidazolidinone

Ghandi, Mehdi,Olyaei, Abolfazl,Salimi, Farshid

, p. 768 - 775 (2007/10/03)

The acid-catalyzed cyclocondensation in refluxing acetonitrile of aqueous glyoxal with N-heteroaryl-N′-phenylureas 4a-f (heteroaryl = 2-thiazolyl, 2-pyrimidinyl, 2-pyrazinyl, 2-pyridinyl, 3-pyridinyl and 2-benzimidazolyl) led to the formation of the corre

Synthesis of N-phenyl-N′-pyrimidylurea derivatives by selenium- or selenium dioxide-catalyzed reductive carbonylation of nitroaromatics

Chen, Jinzhu,Ling, Gang,Lu, Shiwei

, p. 3446 - 3452 (2007/10/03)

Forty unsymmetric N-phenyl-N′-pyrimidylurea derivatives were synthesized in moderate-to-good yields by one-pot reductive carbonylation of nitroaromatics using selenium or selenium dioxide as the catalyst, aminopyrimidine derivatives as co-reagents, and ca

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