33717
硫脲
puriss. p.a., reag. Ph. Eur., ≥99%
别名:
Sulfourea, 硫代尿素
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关于此项目
线性分子式:
NH2CSNH2
化学文摘社编号:
分子量:
76.12
EC Number:
200-543-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
605327
MDL number:
agency
reag. Ph. Eur.
grade
puriss. p.a.
assay
≥99%
ign. residue
≤0.1% (as SO4)
loss
≤0.5% loss on drying
mp
170-176 °C (lit.)
SMILES string
NC(N)=S
InChI
1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
InChI key
UMGDCJDMYOKAJW-UHFFFAOYSA-N
Gene Information
mouse ... Ephx2(13850)
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Application
离液剂；强变性剂。增加蛋白质的溶解性和回收率
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
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
Iris Keren et al.
Science (New York, N.Y.), 339(6124), 1213-1216 (2013-03-09)
Bactericidal antibiotics kill by modulating their respective targets. This traditional view has been challenged by studies that propose an alternative, unified mechanism of killing, whereby toxic reactive oxygen species (ROS) are produced in the presence of antibiotics. We found no
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
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
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