Aspartic acid beta-naphthylamide , CAS No.17139-56-9

CAS: 17139-56-9 Cat. No.: A1026423 PubChem CID: 102456
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A1026423-500mg
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Spezifikationen

Storage
Room temperature
Namen und Kennungen
Kanonisches Lächeln
C1=CC=C2C=C(C=CC2=C1)NC(=O)C(CC(=O)O)N
IUPAC Name
3-amino-4-(naphthalen-2-ylamino)-4-oxobutanoic acid
InChIKey
YRMVHTZHFWHHIU-UHFFFAOYSA-N
INCHI
1S/C14H14N2O3/c15-12(8-13(17)18)14(19)16-11-6-5-9-3-1-2-4-10(9)7-11/h1-7,12H,8,15H2,(H,16,19)(H,17,18)
Isomere SMILES
C1=CC=C2C=C(C=CC2=C1)NC(=O)C(CC(=O)O)N
Alternative CAS-Nummer
635-91-6
PubChem CID
102456
MeSH-Eintrag
alpha-Asp-naphthylamide;Asp-beta-naphthylamide;Asp-NA;aspartic acid beta-naphthylamide;AspNNap

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
KlasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAspartic acid and derivatives
Alternative Parents Alpha amino acid amides  Naphthalenes  N-arylamides  Fatty amides  Secondary carboxylic acid amides  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Aspartic acid or derivatives - Alpha-amino acid amide - Naphthalene - N-arylamide - Fatty acyl - Benzenoid - Fatty amide - Amino acid - Secondary carboxylic acid amide - Carboxamide group - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Aromatic homopolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Molekulargewicht258.269 g/mol
XLogP3-1.300
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass258.1 Da
Monoisotopic Mass258.1 Da
Topological Polar Surface Area92.400 Ų
Heavy Atom Count19
Formal Charge0
Complexity346.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Lösungsrechner
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