O-Acetylserin - ≥97% , CAS No.5147-00-2

CAS: 5147-00-2 Cat. No.: O303851 Summenformel: C₅H₉NO₄ Molekulargewicht: 147.13

GRADE & PURITY ≥97%

Synonyms

A913073 | AKOS006238075 | CHEBI:17981 | MFCD00037771 | O-Acetyl-L-serine (H-L-Ser(Ac)-OH) | Tofacitinib des-(N-oxopropanenitrile)-N-methylbenzyl | Y333RS1786 | (2S)-3-acetyloxy-2-aminopropanoic acid | O-acetyl-l-ser | (2S)-3-(acetyloxy)-2-aminopropanoic a

Storage

Vor Licht geschützt, bei -20°C lagern

Shipped In

Eistruhe + Eispads

Übersicht

Produkt-Beschreibung:

O-Acetylserin (O-Acetyl-L-Serin) ist ein Zwischenprodukt bei der Biosynthese von Cystein in Bakterien und Pflanzen.

Specifications

Synonyme

A913073 | AKOS006238075 | CHEBI:17981 | MFCD00037771 | O-Acetyl-L-serine (H-L-Ser(Ac)-OH) | Tofacitinib des-(N-oxopropanenitrile)-N-methylbenzyl | Y333RS1786 | (2S)-3-acetyloxy-2-aminopropanoic acid | O-acetyl-l-ser | (2S)-3-(acetyloxy)-2-aminopropanoic a

Spezifikationen & Reinheit

≥97%

Storage

Vor Licht geschützt, bei -20°C lagern

Verschickt in

Eistruhe + Eispads

Reinheit

≥97%

Namen und Kennungen

Pubchem Sid

488187183

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488187183

Kanonisches Lächeln

CC(=O)OCC(C(=O)O)N

IUPAC Name

(2S)-3-acetyloxy-2-aminopropanoic acid

InChIKey

VZXPDPZARILFQX-BYPYZUCNSA-N

INCHI

1S/C5H9NO4/c1-3(7)10-2-4(6)5(8)9/h4H,2,6H2,1H3,(H,8,9)/t4-/m0/s1

Isomere SMILES

CC(=O)OC[C@@H](C(=O)O)N

Molekulargewicht

147.13

Reaxy-Rn

1723792

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723792&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Amino acids and derivatives
          • Ebene6 Alpha amino acids and derivatives
            • Ebene7 Alpha amino acids
              • Ebene8 L-alpha-amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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: Dicarboxylic acids and derivatives Carboxylic acid esters Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: L-alpha-amino acid - Dicarboxylic acid or derivatives - Carboxylic acid ester - Amino acid - Carboxylic acid - Hydrocarbon derivative - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Aliphatic acyclic compound
• Beschreibung: 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: acetate ester - acetyl-L-serine

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

Zugehörige Ziele (nicht menschlich)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Slc1a5 Amino acid transporter (271 Activities)

Discover Target: Slc1a5

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: H2O: 32 mg/mL (217.49 mM)
• Empfindlichkeit: light sensitive；heat sensitive
• Molekulargewicht: 147.130 g/mol
• XLogP3: -3.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 147.053 Da
• Monoisotopic Mass: 147.053 Da
• Topological Polar Surface Area: 89.600 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 145.000
• 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

Häufig gestellte Fragen

What is the purity of this product?

This product is supplied at ≥97% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at ?20 °C, protected from light. The material is light-sensitive — keep it in its original opaque or amber container.

How is this product shipped?

This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.

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

The CAS Number is 5147-00-2, the molecular formula is C5H9NO4, and the molecular weight is 147.13 g/mol. InChIKey VZXPDPZARILFQX-BYPYZUCNSA-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.