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Synonyms
(D)-Aspartic acid 4-amide | D70834 | A831678 | RBMGJIZCEWRQES-HSHFZTNMSA-N | A814724 | C4H10N2O4 | DTXSID6048678 | GS-3271 | AM20100419 | D-Asparagine hydrate | NCGC00163330-01 | AKOS015892706 | D-Asparagine monohydrate | Veliparib [USAN:INN] | (2R)-2-ami
Specifications Sinónimos
(D)-Aspartic acid 4-amide | D70834 | A831678 | RBMGJIZCEWRQES-HSHFZTNMSA-N | A814724 | C4H10N2O4 | DTXSID6048678 | GS-3271 | AM20100419 | D-Asparagine hydrate | NCGC00163330-01 | AKOS015892706 | D-Asparagine monohydrate | Veliparib [USAN:INN] | (2R)-2-ami
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488199086 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488199086 Sonrisas canónicas C(C(C(=O)O)N)C(=O)N.O IUPAC Name (2R)-2,4-diamino-4-oxobutanoic acid;hydrate InChIKey RBMGJIZCEWRQES-HSHFZTNMSA-N INCHI 1S/C4H8N2O3.H2O/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);1H2/t2-;/m1./s1 Isómeros SMILES C([C@H](C(=O)O)N)C(=O)N.O WGK Alemania 1 Peso molecular 150.13 Beilstein 1723526 Reaxy-Rn 6234992 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6234992&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
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Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Asparagine and derivatives Alternative Parents D-alpha-amino acids Fatty amides Fatty acids and conjugates Primary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Asparagine or derivatives - Alpha-amino acid - D-alpha-amino acid - Fatty amide - Fatty acyl - Fatty acid - Carboxamide group - Amino acid - Primary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as asparagine and derivatives. These are compounds containing asparagine or a derivative thereof resulting from reaction of asparagine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. External Descriptors Not available 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.
Estructura 3D Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in water (35 g/L at 20°C). Rotación específica [α] -31° (C=10,HCl(1+3)) Punto de fusión (°C) 280°C Peso molecular 150.130 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 3 Exact Mass 150.064 Da Monoisotopic Mass 150.064 Da Topological Polar Surface Area 107.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 134.000 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 2
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