2-Mercaptothiazoline

2-Mercaptothiazoline
  • CAS No.:96-53-7
Other grades of this product :
2-Mercaptothiazoline Basic information
Product Name:2-Mercaptothiazoline
Synonyms:2-MERCAPTOTHIAZOLINE 98%;2-Thiothiazoline;2-Mercaptothiazoline~94%;2-Mercaptothiazoline ,98%;H4MT;Medical interMediates;2-thiazolinethiol;2-MERCAPTOTHIAZOLIDINE
CAS:96-53-7
MF:C3H5NS2
MW:119.21
EINECS:202-512-1
Product Categories:Pyrans;API intermediates;fine chemical;pharmaceutical intermediate
Mol File:96-53-7.mol
2-Mercaptothiazoline Chemical Properties
Melting point 100-105 °C(lit.)
Boiling point 176-178 °C(Press: 0.25 Torr)
density 1.235 (estimate)
refractive index 1.4826 (estimate)
storage temp. Store below +30°C.
pka13.01±0.20(Predicted)
form Fine Crystalline Powder
color White to beige
PH6-7 (10g/l, H2O, 20℃)
Water Solubility SOLUBLE IN HOT WATER
BRN 106332
InChIKeyWGJCBBASTRWVJL-UHFFFAOYSA-N
CAS DataBase Reference96-53-7(CAS DataBase Reference)
NIST Chemistry Reference2-Thiazolidinethione(96-53-7)
EPA Substance Registry System2-Thiazolidinethione (96-53-7)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 24/25
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS XJ6122000
TSCA Yes
HazardClass 6.1(b)
PackingGroup III
HS Code 29341000
ToxicityLD50 orally in Rabbit: 300 mg/kg
MSDS Information
ProviderLanguage
2-Mercaptothiazoline English
SigmaAldrich English
ACROS English
ALFA English
2-Mercaptothiazoline Usage And Synthesis
Chemical Propertieswhite to beige fine crystalline powder
Usesmedicament.;medical agent; brightening agent
Uses2-Mercaptothiazoline is an antithyroid agent that strongly reduces thyroid hormone levels. 2-Mercaptothiazoline is also used as an intermediate in the preparation of pesticides and other biologically active compounds.
Uses2-Mercaptothiazoline, is used in the chain-lengthening of alkyl halides by trans-iodopropenylenation. 2-Mercaptothiazoline is an antithyroid agent that strongly reduces thyroid hormone levels. 2-Mercaptothiazoline is also used as an intermediate in the preparation of biologically active compounds. It is also used as a tool for highly selective chiral synthesis of penam- and carbapenam-type β-lactam antibiotics.
Purification MethodsPurify the thiol by dissolution in aqueous alkali, precipitation by addition of HCl and then recrystallisation from H2O (as needles). [IR: Flett J Chem Soc 347 1953 and Mecke et al. Chem Ber 90 975, Gabriel & Stelzner Chem Ber 28 2931 1895, Beilstein 27 III/IV 2540.]

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