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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Thiazolidine, hydrochloride

C1NCCS1.Cl Request for Quotation
Chemical Name: Thiazolidine, hydrochloride
CAS Number: 14446-47-0
Product Number: AG001JKR(AGN-PC-0NIZJ7)
Synonyms:
MDL No:
Molecular Formula: C3H8ClNS
Molecular Weight: 125.6203

Identification/Properties

Computed Properties
Molecular Weight:
125.614g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
125.007g/mol
Monoisotopic Mass:
125.007g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
30.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Thiazolidine hydrochloride is a versatile compound widely used in chemical synthesis as a key building block for the formation of various heterocyclic compounds. Its ability to undergo facile condensation reactions with aldehydes or ketones enables efficient access to pharmacologically important structures. Thiazolidine hydrochloride serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Its application in organic chemistry extends to the development of novel synthetic routes and the preparation of diverse molecular architectures with potential therapeutic significance.