M6204
2-巯基噻唑啉
98%
别名:
2-巯基-2-噻唑啉
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选择尺寸
关于此项目
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
Taro Hase et al.
Urology, 60(3), 542-547 (2002-09-28)
To investigate the expression of peroxisome proliferator activator-receptor (PPAR)-alpha, beta, and gamma in human testicular cancer (TC) and normal testicular (NT) tissues, as well as the effects of the PPAR-gamma ligand. Recent studies have demonstrated that PPAR-gamma is expressed in
Cestmír Konák et al.
Langmuir : the ACS journal of surfaces and colloids, 24(14), 7092-7098 (2008-06-12)
Vesicles bearing either cationic (amino) groups or zwitterionic (amino acid) groups on the surface were coated with a reactive multivalent hydrophilic N-(2-hydroxypropyl)methacrylamide polymer (PHPMA) and its positively charged analogue (3 mol % quaternary ammonium groups), both having reactive thiazolidine-2-thione (TT)
J C Thomes et al.
Japanese journal of pharmacology, 58(3), 201-207 (1992-03-01)
2-Thiazoline-2-thiol is an antithyroid agent that strongly reduces thyroid hormone levels. Synthesis of these hormones is catalyzed in vivo by thyroid peroxidase. The interaction of this drug with molecular iodine and its effect on peroxidase activity were investigated. Iodine and
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
Chem. Abstr., 108, 37417r-37417r (1988)
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