30-1940
Thiourea
JIS special grade, ≥98.0%
Sinónimos:
Sulfourea, Thiocarbamide
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About This Item
Fórmula lineal:
NH2CSNH2
Número de CAS:
Peso molecular:
76.12
Beilstein:
605327
Número MDL:
Código UNSPSC:
12352300
ID de la sustancia en PubChem:
En este momento no podemos mostrarle ni los precios ni la disponibilidad
Productos recomendados
grado
JIS special grade
Ensayo
≥98.0%
Formulario
solid
disponibilidad
available only in Japan
mp
170-176 °C (lit.)
cadena SMILES
NC(N)=S
InChI
1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
Clave InChI
UMGDCJDMYOKAJW-UHFFFAOYSA-N
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Aplicación
Chaotropic agent; strong denaturant. Increases solubility and recovery of proteins
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 2
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Shrinivas Venkataraman et al.
Macromolecular rapid communications, 34(8), 652-658 (2013-03-14)
Readily water-soluble PEGylated amphiphiles containing bis-thiourea-based molecular recognition units at the interface of hydrophobic and hydrophilic blocks are developed. Self-assembly of these amphiphiles is found to be dependent on the exact chemical composition of the hydrophobic component. Elongated, spherical, and
Mathieu P Lalonde et al.
Journal of the American Chemical Society, 135(5), 1891-1894 (2013-01-17)
A highly enantio- and diastereoselective synthesis of indolo- and benzoquinolizidine compounds has been developed through the formal aza-Diels-Alder reaction of enones with cyclic imines. This transformation is catalyzed by a new bifunctional primary aminothiourea that achieves simultaneous activation of both
Mireille Vonlanthen et al.
The Journal of organic chemistry, 78(8), 3980-3988 (2013-03-09)
Proof that sulfur is a viable reporting element for the development of fluorescent chemosensors for metal ions is presented. To date, the majority of metal-responsive fluorescent chemosensors have relied on metal-nitrogen coordination to provide a fluorescence response, most commonly by
Yoshiji Takemoto
Chemical & pharmaceutical bulletin, 58(5), 593-601 (2010-05-13)
We have developed several multifunctional thiourea catalysts bearing a tertiary amine or an 1,2-amino alcohol in expectation of their synchronous activation of a nucleophile and an electrophile through both acid-base and hydrogen-bonding interactions. From these studies, it was revealed that
Ai-Fang Li et al.
Chemical Society reviews, 39(10), 3729-3745 (2010-08-26)
This critical review highlights recent advances in the structurally modified (thio)urea-based receptors for anion complexation and sensing. Modifications of the (thio)urea structure are aimed at a better anion binding in terms of higher binding constant, anion selectivity and feasibility. Major
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