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.)

Flash point:

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

• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS

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(504-78-9)Related Product Information

• 1,2,3,4-TETRAHYDROISOQUINOLINE
• TETRAHYDROTHIOPYRAN-4-OL 97
• TETRAHYDRO-THIOPHEN-3-OL
• 2H-Thiopyran-4-methanol, tetrahydro-
• 2-Thiophenecarboxylic acid, tetrahydro-
• Tetrahydrothiopyran-4-one oxiMe
• 3-THIOPHENAMINE, TETRAHYDRO-
• Thiazolidine, hydrochloride (1:1)
• TETRAHYDROTHIOPYRAN-4-CARBONITRILE
• 2H-Thiopyran-4-carboxylicacid,tetrahydro-(9CI)
• Tetrahydro-2H-thiopyran-4-amine
• tetrahydrothiophen-3-yl 4-methylbenzenesulfonate
• 1,1-Dioxo-tetrahydro-thiopyran-4-one
• Tetrahydrothiopyran-4-one
• Tetrahydrothiophen-3-one
• Tetrahydrothiopyran-4-carbaldehyde
• Tetryzoline
• bis(2,3-epoxypropyl) cyclohex-4-ene-1,2-dicarboxylate