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关于此项目
经验公式(希尔记法):
C4H5NOS2
化学文摘社编号:
分子量:
147.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1210145
Application
可用于 Barton 反应,通过对应酯的脱羧重排生成碳自由基。
General description
3-Hydroxy-4-methyl-2(3H)-thiazolethione (HMTT) is a cyclic thiohydroxamic acid. It forms divalent complexes with the first-row d-block elements Co-Zn. Hydrated form of HMTT exhibits enhanced thermal stability and solubility compared with the anhydrous form. HMTT possess a chelating unit similar to pyrithione. Solid state chemistry of HMTT and its complexes with d-block elements has been reported.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Synthesis and X-ray crystal structures of bis (3-hydroxy-4-methyl-2 (3H)-thiazolethiolato-S 2, O) bis (dimethylsulfoxide-O) M, M= cobalt (II) and nickel (II).
Bond AD and Jones W.
Transition Met. Chem. (London), 27(4), 407-410 (2002)
Solid-state study of cyclic thiohydroxamic acids: 1-hydroxy-2 (1H)-pyridinethione and 3-hydroxy-4-methyl-2 (3H)-thiazolethione.
Bond AD and Jones W.
Journal of Physical Organic Chemistry, 13(7), 395-404 (2000)
Divalent complexes of 3-hydroxy-4-methyl-2 (3H)-thiazolethione with Co-Zn: synthesis, X-ray crystal structures and the structure-directing influence of C-HS interactions.
Bond AD and Jones W.
J. Chem. Soc., Dalton Trans., 20, 3045-3051 (2001)
Journal of the Chemical Society. Perkin Transactions 1, 39-39 (1986)
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