(S)-Thiazolidine-4-carboxylic acid

A summary of the most common chemical descriptors (InChI Key and SMILES codes) for (S)-Thiazolidine-4-carboxylic acid are summarized together with 3D and 2D structures and relevant physico-chemical properties.

What is the (S)-Thiazolidine-4-carboxylic acid?

The molecule (S)-Thiazolidine-4-carboxylic acid presents a molecular formula of C4H7NO2S and its IUPAC name is (4S)-1,3-thiazolidine-4-carboxylic acid.

S-Thiazolidine-4-carboxylic acid is a molecule with the chemical formula C4H5NO2S. It is a white solid that is soluble in water and organic solvents. It is used as a reagent in organic synthesis and as a pharmaceutical intermediate..

3D structure

Cartesian coordinates

Geometry of (S)-Thiazolidine-4-carboxylic acid in x, y and z coordinates (Å units) to copy/paste elsewhere. Generated with Open Babel software.

2D drawing

 

(S)-Thiazolidine-4-carboxylic acid DZLNHFMRPBPULJ-GSVOUGTGSA-N chemical compound 2D structure molecule svg
(S)-Thiazolidine-4-carboxylic acid

 

Molecule descriptors

 
IUPAC name(4S)-1,3-thiazolidine-4-carboxylic acid
InChI codeInChI=1S/C4H7NO2S/c6-4(7)3-1-8-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m1/s1
InChI KeyDZLNHFMRPBPULJ-GSVOUGTGSA-N
SMILESO=C(O)[C@H]1CSCN1

Other names (synonyms)

IUPAC nomenclature provides a standardized method for naming chemical compounds. Although this system is widely used in chemistry, many chemical compounds have also other names commonly used in different contexts. These synonyms can come from a variety of sources and are used for a variety of purposes.

One common source of synonyms for chemical compounds is the common or trivial names, assigned on the basis of appearance, properties, or origin of the molecule.

Another source of synonyms are historical or obsolete names employed in the past, however replaced nowadays by more modern or standardized names.

In addition to common and historical names, chemical compounds may also have synonyms that are specific to a particular field or industry.

  • (4S)-1,3-thiazolidine-4-carboxylic acid
  • (4S)-4-thiazolidinecarboxylic acid
  • (S)-(+)-4-thiazolidinecarboxylic acid
  • (S)-4-Thiazolidinecarboxylic acid
  • (S)-Thiazolidine-4-carboxylic acid
  • (S)-Thiazolidine-4-carboxylicacid
  • (S)-timonacic
  • 4-Thiazolidinecarboxylic acid, (4S)-
  • 4-Thiazolidinecarboxylic acid, (S)-
  • 4-Thiazolidinecarboxylic acid, D-
  • 45521-09-3
  • 45521-09-3 (S-isomer)
  • 5VQB2231Z8
  • A918350
  • AS-14795
  • Acide D thiazolidine carboxylique-4
  • CS-0097362
  • D-THIOPROLINE
  • D-Thiaproline
  • D-Thiazolidine-4-carboxylic acid
  • H-D-THZ-OH
  • MFCD00137425
  • O10231
  • Q27133347
  • Timonacic, (S)-

Reference codes for other databases

There exist several different chemical codes commonly used in orded to identify molecules:
  • ZINC967474
  • UNII-5VQB2231Z8
  • AKOS000103753
  • DTXSID70196545
  • CHEBI:64562
  • EINECS 256-240-3
  • SCHEMBL15546

Physico-Chemical properties

IUPAC name(4S)-1,3-thiazolidine-4-carboxylic acid
Molecular formulaC4H7NO2S
Molecular weight133.169
Melting point (ºC)
Boiling point (ºC)
Density (g/cm3)
Molar refractivity35.31
LogP0.1
Topological polar surface area74.6

LogP and topological polar surface area (TPSA) values were estimated using Open Babel software.

The n-octanol/water partition coeficient (Kow) data is applied in toxicology and drug research. Kow values are used, to guess the environmental fate of persistent organic pollutants. High partition coefficients values, tend to accumulate in the fatty tissue of organisms. Molecules with a log(Kow) (or LogP) greater than 5 are considered to bioaccumulate.

TPSA values are the sum of the surface area over all polar atoms or molecules, mainly oxygen and nitrogen, also including hydrogen atoms.

In medicinal chemistry, TPSA is used to assess the ability of a drug to permeabilise cells.

For molecules to penetrate the blood-brain barrier (and act on receptors in the central nervous system), TPSA values below 90 Å2 are required. Thus, molecules with a polar surface area greater than 140 Å2 tend to be poorly permeable to cell membranes.