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ChemicalBook--->CAS DataBase List--->179337-57-6

179337-57-6

179337-57-6 Structure

179337-57-6 Structure
IdentificationBack Directory
[Name]

3-Azetidinethiol, 1-(4,5-dihydro-2-thiazolyl)-, monohydrochloride
[CAS]

179337-57-6
[Synonyms]

TibipeneMSideChian
Tebipenem Impurity 2
TebipeneM Side Chain
TebipenaM Side Chain
Tebipenem intermediate
Side Chain of TebipeneM
Taibipeinan side chains
Tebipenem ester intermediate
Side Chain of Tebipenem pivoxil
1-(4,5-dihydro-1,3-thiazol-2-yl)azetidine-3-thiol
2-(3-Mercaptoazetidin-1-yl)-2-thiazoline hydrochloride
3-Mercapto-1-(1,3-thiazolin-2-yl)azetidine hydrochloride
3-MERCAPTO-1-(1,3-THIAZOLIN-2-YL)ZAETIDINE HYDROCHLORIDE
1-(4,5-Dihydro-2-thiazolyl)-3-azetidinethiol hydrochloride
1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride
1-(4,5-dihydro-1,3-thiazol-2-yl)azetidine-3-thiol,hydrochloride
3-Azetidinethiol, 1-(4,5-dihydro-2-thiazolyl)-, monohydrochloride
3-Azetidinethiol, 1-(4,5-dihydro-2-thiazolyl)-, hydrochloride (1:1)
3-Azetidinethiol, 1-(4,5-dihydro-2-thiazolyl)-, monohydrochloride USP/EP/BP
[EINECS(EC#)]

1308068-626-2
[Molecular Formula]

C6H11ClN2S2
[MDL Number]

MFCD18072489
[MOL File]

179337-57-6.mol
[Molecular Weight]

210.748
Chemical PropertiesBack Directory
[Melting point ]

134-136℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

Chloroform (Sparingly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
[InChI]

InChI=1S/C6H10N2S2.ClH/c9-5-3-8(4-5)6-7-1-2-10-6;/h5,9H,1-4H2;1H
[InChIKey]

WLQPQHGYHHHITD-UHFFFAOYSA-N
[SMILES]

N1(C2=NCCS2)CC(S)C1.[H]Cl
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P231-P222-P261-P305+P351+P338-P403+P233-P422-P501
Hazard InformationBack Directory
[Uses]

1-(4,5-Dihydro-2-thiazolyl)-3-azetidinethiol Hydrochloride is used as a reagent in the synthesis of Tebipenem Tetrahydrate (T012840); the active metabolite of Tebipenem Pivoxil (T012900) that shows excellent bactericidal activity against β-lactamase-nonproducing, ampicillin-resistant isolates.
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