P7629
N-Phenylthiourea
≥98%
동의어(들):
1-Phenyl-2-thiourea, PTU, Phenylthiocarbamide
조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5NHCSNH2
CAS 번호:
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
InChI key
FULZLIGZKMKICU-UHFFFAOYSA-N
InChI
1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)
SMILES string
NC(=S)Nc1ccccc1
assay
≥98%
form
powder
Quality Level
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Oral - Skin Sens. 1
저장 등급
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
No data available
flash_point_c
No data available
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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)
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)
Solvent-free synthesis of luminescent copper (I) coordination polymers with thiourea derivatives
Grifasi F, et al.
Crystal Growth & Design, 15, 2929-2939 (2015)
Stephen Wooding et al.
Chemical senses, 35(8), 685-692 (2010-06-17)
The perceived bitterness of cruciferous vegetables such as broccoli varies from person to person, but the functional underpinnings of this variation are not known. Some evidence suggests that it arises, in part, from variation in ability to perceive goitrin (5-vinyloxazolidine-2-thione)
Panagiotis Symvoulidis et al.
Nature methods, 14(11), 1079-1082 (2017-10-03)
A long-standing objective in neuroscience has been to image distributed neuronal activity in freely behaving animals. Here we introduce NeuBtracker, a tracking microscope for simultaneous imaging of neuronal activity and behavior of freely swimming fluorescent reporter fish. We showcase the
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