102-03-4

Basic information

• Product Name: N-ACETYL-N'-PHENYLUREA
• Synonyms: 1-acetyl-3-phenyl-ure;n-((phenylamino)carbonyl)-acetamid;phenylureidoaceticacid;N-PHENYL-N'-ACETYLUREA;N-ACETYL-N'-PHENYLUREA;SYM-ACETYLPHENYL UREA;1-acetyl-3-phenylurea;N-[(Phenylamino)carbonyl]acetamide
• CAS NO: 102-03-4
• Molecular Formula: C₉H₁₀N₂O₂
• Molecular Weight: 178.19
• EINECS: 202-999-0
• Mol File: 102-03-4.mol
• Article Data: 7

Chemical Properties

• Melting Point: 183 °C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.229g/cm³
• Refractive Index: 1.587
• PKA: 12.45±0.70(Predicted)
• CAS DataBase Reference: N-ACETYL-N'-PHENYLUREA(CAS DataBase Reference)
• NIST Chemistry Reference: N-ACETYL-N'-PHENYLUREA(102-03-4)
• EPA Substance Registry System: N-ACETYL-N'-PHENYLUREA(102-03-4)

Safety Data

• Hazardous Substances Data: 102-03-4(Hazardous Substances Data)

Usage

Uses

N-Acetyl-N’-phenylurea is used in preparation of ureas by condensation of Carbamates with Amines.

InChI:InChI=1/C9H10N2O2/c1-7(12)10-9(13)11-8-5-3-2-4-6-8/h2-6H,1H3,(H2,10,11,12,13)

Upstream product

• 64-10-8 phenyl carbamate 
• 108-24-7 acetic anhydride 
• 622-34-4 1-phenylcyanamide 
• 60-35-5 acetamide 
• 103-71-9 phenyl isocyanate 
• 598-49-2 N-chloroacetamide 
• 591-07-1 acetylurea 
• 62-53-3 aniline 
• 2911-21-9 2,4-dioxo-6-methyl-3,4-dihydro-2H-1,3-oxazine 
• 56-23-5 tetrachloromethane 
• 2597-54-8 ethyl acetylcarbamate 
• 1132-44-1 1-acetyl-3-phenylthiourea 
• 55-21-0 benzamide 
• 15837-45-3 6-amino-1-phenyluracil 

Downstream Products

• 603-54-3 N,N-diphenylurea 
• 67080-96-0 N-acetyl-N'-(4-sulfamoyl-phenyl)-urea 
• 5657-41-0 N³-(4-sulfamoylphenyl)urea 
• 32767-01-4 N-acetyl-N'-(4-bromo-phenyl)-urea 
• 67080-67-5 N-acetylcarbamoyl-sulfanilyl chloride 

Relevant articles and documents

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Synthesis of N-benzothiazol-2-yl-amides by an iron-catalyzed oxidative C(sp2)-H functionalization

Catalytic synthesis of N-benzothiazol-2-yl-amides from 1-acyl-3-(phenyl) thioureas was achieved in the presence of an iron catalyst through C(sp 2)-H functionalization and C-S bond formation. Various N-benzothiazol-2-yl-amides were selectively obtained in good yields. Georg Thieme Verlag Stuttgart, New York.

PYRIDO [2, 3-D] PYRIMIDINES AS WNT ANTAGONISTS FOR TREATMENT OF CANCER AND ARTHRITIS

Compounds according to the general formula (I) their solvates, hydrates, esters and pharmaceutically acceptable salts, their use for modulating the Wnt signalling pathway activity and their use as a medicament, preferably for the treatment of cancer