P7629
N-Phenylthiourea
≥98%
Synonym(s):
1-Phenyl-2-thiourea, PTU, Phenylthiocarbamide
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About This Item
Linear Formula:
C6H5NHCSNH2
CAS Number:
Molecular Weight:
152.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-151-2
Beilstein/REAXYS Number:
907309
MDL number:
Assay:
≥98%
Form:
powder
Quality Level
assay
≥98%
form
powder
mp
145-150 °C (lit.)
SMILES string
NC(=S)Nc1ccccc1
InChI
1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)
InChI key
FULZLIGZKMKICU-UHFFFAOYSA-N
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
General description
N-Phenylthiourea, also known as phenylthiocarbamide (PTC) is an organosulfur thiourea containing a phenyl ring, that is commonly used as a reactant to synthesis N- phenylformamidinoformamidinothiocarbamide.
Application
N-Phenylthiourea can be used as a reactant to synthesize:
- Thiazoles via solvent- and catalyst-free condensation with halo ketones.
- Formamidine disulfides via oxidation.
- Luminescent copper(I) cyanide-based coordination polymers.
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Danger
hcodes
Hazard Classifications
Acute Tox. 1 Oral - Skin Sens. 1
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
flash_point_f
No data available
flash_point_c
No data available
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Microwave assisted solvent-free synthesis of N-phenyl-4-(pyridin-4-yl) thiazoles and their drug-likeness studies
Kukade M, et al.
Journal of the Indian Chemical Society, 99, 100509-100509 (2022)
Oxidative conversion of thiourea and N-substituted thioureas into formamidine disulfides with acidified chloramine-T: a kinetic and mechanistic approach
Shubha J, et al.
Journal of Sulfur Chemistry, 30, 490-499 (2009)
Solvent-free synthesis of luminescent copper (I) coordination polymers with thiourea derivatives
Grifasi F, et al.
Crystal Growth & Design, 15, 2929-2939 (2015)