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经验公式(希尔记法):
C3H5NS2
化学文摘社编号:
分子量:
119.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-512-1
Beilstein/REAXYS Number:
106332
MDL number:
产品名称
2-巯基噻唑啉, 98%
InChI
1S/C3H5NS2/c5-3-4-1-2-6-3/h1-2H2,(H,4,5)
InChI key
WGJCBBASTRWVJL-UHFFFAOYSA-N
SMILES string
S=C1NCCS1
assay
98%
mp
100-105 °C (lit.)
Quality Level
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Application
用于高选择性手性合成青霉烷和碳青霉烷类 β-内酰胺抗生素的工具。
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Chem. Abstr., 108, 37417r-37417r (1988)
Yahia N Mabkhot et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-01)
A series of new thiazoline derivatives were synthesized. Structure analyses were accomplished employing 1H-NMR, 13C-NMR, X-ray and MS techniques. The in vitro antitumor activities were assessed against human hepatocellular carcinoma (HepG-2) and colorectal carcinoma (HCT-116) cell lines. The results revealed
Stud. Org. Chem., 28, 57-57 (1987)
Denis L Guerra et al.
Journal of hazardous materials, 183(1-3), 81-86 (2010-08-03)
The synthetic imogolite sample was used for organofunctionalization process with 2-mercaptothiazoline (MTZ). The compound 2-mercaptothiazoline was anchored onto imogolite surface by heterogeneous route. Due to the increment of basic centers attached to the pendant chains the dye adsorption capability of
R B Greenwald et al.
Bioconjugate chemistry, 7(6), 638-641 (1996-11-01)
A novel PEG linker that employs a thiazolidine-2-thione group has been synthesized. Kinetic studies done on this compound demonstrate a relatively long half-life compared to those of traditional succinimidyl linkers. This new PEG derivative reacts with proteins under mild conditions
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