ChemicalBook--->CAS DataBase List--->504-78-9

504-78-9

504-78-9 Structure

504-78-9 Structure
IdentificationMore
[Name]

THIAZOLIDINE
[CAS]

504-78-9
[Synonyms]

TETRAHYDROTHIAZOLE
THIAZOLIDINE
1,3-Thiazolidine
1-Thia-3-azacyclopentane
THIAZOLIDINE
TETRAHYDROTHIAZOLE
Thiazolidine ,98%
[EINECS(EC#)]

208-002-5
[Molecular Formula]

C3H7NS
[MDL Number]

MFCD00005211
[Molecular Weight]

89.16
[MOL File]

504-78-9.mol
Chemical PropertiesBack Directory
[Appearance]

clear colorless liquid
[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)
[form ]

Liquid
[pka]

8.84±0.20(Predicted)
[color ]

Clear colorless
[Detection Methods]

GC
[InChIKey]

OGYGFUAIIOPWQD-UHFFFAOYSA-N
[LogP]

-1.725 (est)
[CAS DataBase Reference]

504-78-9(CAS DataBase Reference)
[Storage Precautions]

Store under nitrogen
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[RIDADR ]

UN 1993 3/PG 3
[WGK Germany ]

3
[RTECS ]

XJ5123700
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29341000
Raw materials And Preparation ProductsBack Directory
[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
Hazard InformationBack Directory
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

THIAZOLIDINE(504-78-9)MS
THIAZOLIDINE(504-78-9)1HNMR
THIAZOLIDINE(504-78-9)13CNMR
THIAZOLIDINE(504-78-9)IR1
THIAZOLIDINE(504-78-9)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Thiazolidine, 98%(504-78-9)
[Alfa Aesar]

Thiazolidine, 97%(504-78-9)
[Sigma Aldrich]

504-78-9(sigmaaldrich)
[TCI AMERICA]

Thiazolidine,>98.0%(GC)(T)(504-78-9)
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