L-Thiaproline - ≥98%(HPLC) , CAS No.34592-47-7

CAS: 34592-47-7 Cat. No.: T137734 Formula: C₄H₇NO₂S Peso molecolare: 133.17 Beilstein Registry Number: 81065 Numero EC: 252-106-3 PubChem CID: 93176

GRADE & PURITY ≥98%(HPLC)

Synonyms

4-Thiazolidinecarboxylic acid, (R)- | (R)-timonacic | Syrigin | TIMONACIC, (-)- | DTXSID3046536 | BDBM50357232 | L-Thioproline | Thioproline, L- | (R)-(-)-4-Thiazolidinecarboxylic acid | AKOS016346321 | Styryl carbinol | CAS-34592-47-7 | CCRIS 3646 | DTXC

Storage

Room temperature,Argon charged

Shipped In

Normal

Panoramica

L-4-Thiazolidinecarboxylic acid has been used in peptide coupling reactions.

Specifications

Sinonimi

4-Thiazolidinecarboxylic acid, (R)- | (R)-timonacic | Syrigin | TIMONACIC, (-)- | DTXSID3046536 | BDBM50357232 | L-Thioproline | Thioproline, L- | (R)-(-)-4-Thiazolidinecarboxylic acid | AKOS016346321 | Styryl carbinol | CAS-34592-47-7 | CCRIS 3646 | DTXC

Specifiche e purezza

≥98%(HPLC)

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Purezza

≥98%(HPLC)

Nomi e identificatori

• Pubchem Sid: 504756175
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756175
• Sorrisi canonici: C1C(NCS1)C(=O)O
• IUPAC Name: (4R)-1,3-thiazolidine-4-carboxylic acid
• InChIKey: DZLNHFMRPBPULJ-VKHMYHEASA-N
• INCHI: 1S/C4H7NO2S/c6-4(7)3-1-8-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m0/s1
• Isomeri SMILES: C1[C@H](NCS1)C(=O)O
• WGK Germania: 3
• RTECS: XJ5425500
• PubChem CID: 93176
• Peso molecolare: 133.17
• Beilstein: 81065
• Reaxy-Rn: 81065

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acids
              • Level8 L-alpha-amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
• Direct Parent: L-alpha-amino acids
• Alternative Parents: Thiazolidines Amino acids Thiohemiaminal derivatives Monocarboxylic acids and derivatives Dialkylthioethers Dialkylamines Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: L-alpha-amino acid - Thiazolidine - Amino acid - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Thioether - Hemithioaminal - Dialkylthioether - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Amine - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
• External Descriptors: thiazolidinemonocarboxylic acid - thioproline

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)

Discover Target: SLC36A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Air sensitive
• Rotazione specifica [α]: -200° (C=1,1mol/L NaOH sol.)
• Punto di fusione (°C): 192-200°C
• Peso molecolare: 133.170 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 133.02 Da
• Monoisotopic Mass: 133.02 Da
• Topological Polar Surface Area: 74.600 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 106.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Domande frequenti

What is the purity of this product, and how is it determined?

This product is supplied at ≥98% purity, determined by HPLC. Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 34592-47-7, the molecular formula is C4H7NO2S, and the molecular weight is 133.17 g/mol. InChIKey DZLNHFMRPBPULJ-VKHMYHEASA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.