THIAZOLIDINE

THIAZOLIDINE Basic information

Product Name:	THIAZOLIDINE
Synonyms:	Thiazolidine, 98% 1GR;Ring Parent;Thiazolidine ,98%;Thiazolidine 95%;THIAZOLIDINE TETRAHYDROTHIAZOLE;THIAZOLIDINE;TETRAHYDROTHIAZOLE;1-Thia-3-azacyclopentane
CAS:	504-78-9
MF:	C3H7NS
MW:	89.16
EINECS:	208-002-5
Product Categories:	Heterocyclic Compounds;Building Blocks;Heterocyclic Building Blocks;Thiazolines/Thiazolidines
Mol File:	504-78-9.mol

THIAZOLIDINE Chemical Properties

Boiling point	72-75 °C/25 mmHg (lit.)
density	1.131 g/mL at 25 °C (lit.)
refractive index	n20/D 1.5508(lit.)
Fp	133 °F
storage temp.	under inert gas (nitrogen or Argon) at 2–8 °C
solubility	Chloroform (Sparingly), Methanol (Slightly)
pka	8.84±0.20(Predicted)
form	Liquid
color	Clear colorless
InChIKey	OGYGFUAIIOPWQD-UHFFFAOYSA-N
LogP	-1.725 (est)
CAS DataBase Reference	504-78-9(CAS DataBase Reference)

Safety Information

Hazard Codes	C
Risk Statements	34
Safety Statements	45-36/37/39-26
RIDADR	UN 1993 3/PG 3
WGK Germany	3
RTECS	XJ5123700
HazardClass	3
PackingGroup	III
HS Code	29341000

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English

THIAZOLIDINE Usage And Synthesis

Chemical Properties	clear colorless liquid
Chemical Properties	Thiazolidines are a class of hetrocyclic organic compounds having a 5 membered saturated ring with a thio ether group at 1 position and an amine group in the 3 position. It is sulfur analogue of oxazolidine. Thiazolidines may be synthesized by a condensation reaction between a thiol and an aldehyde or ketone. It is a reversible reaction. Therefore many thiazolidines are labile towards hydrolysis in aqueous solution. Hydrolysis of the thiazolidine generates the thiol and an aldehyde from which it was synthesized.
Uses	Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides.
Definition	ChEBI: 1,3-thiazolidine is a thiazolidine.

THIAZOLIDINE Preparation Products And Raw materials

Raw materials	Formaldehyde-->Cysteamine hydrochloride
Preparation Products	2-Mercaptobenzothiazole-->Nizatidine-->Fosthiazate-->3-(-Hydroxyphenethyl)-2-imino thiazolidine-->(2S)-4-Oxo-2-(3-thiazolidinylcarbonyl)-1-pyrrolidinecarboxylic acid tert-butyl ester-->4-[[(2-aminoethyl)thio]methyl]-5-methylimidazole

L-THIOPROLINE 3-(2-AMINO-ETHYL)-THIAZOLIDINE-2,4-DIONE 3-(4-CHLOROPHENYL)SPIRO[1,3-THIAZOLIDINE-2,3'-INDOLINE]-4,7-DIONE LABOTEST-BB LT00112326 N-Aminorhodanine 2-(2-THIENYL)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID 3-(4-CHLORO-BENZOYL)-2-P-TOLYL-THIAZOLIDINE-4-CARBOXYLIC ACID tetramisole 3-METHYLRHODANINE 3-(3-CHLORO-BENZOYL)-2-P-TOLYL-THIAZOLIDINE-4-CARBOXYLIC ACID Guaisteine 2,2-Dimethylthiazolidine Rhodanine 5-[1-(4-CHLORO-PHENYL)-METH-(Z)-YLIDENE]-2-THIOXO-THIAZOLIDIN-4-ONE 5-(3-HYDROXY-BENZYLIDENE)-2-THIOXO-THIAZOLIDIN-4-ONE AKOS B029114 AKOS B029103 3-(5-OXO-PYRROLIDINE-2-CARBONYL)-THIAZOLIDINE-4-CARBOXYLIC ACID

Email:[email protected] [email protected]

Copyright © 2024 Mywellwork.com All rights reserved.