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Key Documents

Outros documentos

30-1940

Sigma-Aldrich

Thiourea

JIS special grade, ≥98.0%

Sinônimo(s):

Sulfourea, Thiocarbamide

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About This Item

Fórmula linear:
NH2CSNH2
Número CAS:
62-56-6
Peso molecular:
76.12
Beilstein:
605327
Número MDL:
MFCD00008067
Código UNSPSC:
12352300
ID de substância PubChem:
329753346

grau

JIS special grade

Ensaio

≥98.0%

forma

solid

disponibilidade

available only in Japan

pf

170-176 °C (lit.)

cadeia de caracteres SMILES

NC(N)=S

InChI

1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)

chave InChI

UMGDCJDMYOKAJW-UHFFFAOYSA-N

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Aplicação

Chaotropic agent; strong denaturant. Increases solubility and recovery of proteins

Palavra indicadora

Warning

Frases de perigo

H302,H351,H361fd,H411

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

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Elaine M Boyle et al.
The Journal of organic chemistry, 78(17), 8312-8319 (2013-08-01)
Thiourea-functionalized Tröger's base receptors 1 and 2 have been synthesized and evaluated as novel for the recognition of anions. Receptor 2 gave rise to significant changes in the absorption spectrum upon titration with AcO(-) and H2PO4(-) and acted as a
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
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
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
David Weisbrod et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(18), E1685-E1694 (2013-04-17)
Proper expression and function of the cardiac pacemaker is a critical feature of heart physiology. Two main mechanisms have been proposed: (i) the "voltage-clock," where the hyperpolarization-activated funny current If causes diastolic depolarization that triggers action potential cycling; and (ii)
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