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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Aminopyrazine - ≥99% , CAS No.5049-61-6
Disponível para encomenda
Synonyms
Pyrazine, 2-amino-|pyrazineamine|2-(1,3-dioxoisoindolin-2-yl)ethyl acetate|Aminopyrazine|amino-pyrazine|AMINO PYRAZINE|1,2-Dihydro-2-iminopyrazine|3-AMINOPYRAZINE|iminopyrazine|Octanoic acid, 2-methylpropyl ester|2-Aminopyrazine|PYRIDINE,2-CHLORO-3-NITRO-|2-Pyrazinamine|pyrazin-2-ylamine|Pyrazin-2-yl-amine|Pyrazine,2-dihydro-2-imino-|1-(p-Chlorophenyl)-2-methyl-2-propanol|1-[4-(pentyloxy)phenyl]ethan-1-one|Pyrazinamine|Pyrazinamine-|Pyrazine, amino-|2-Pyrazinamine #|4-(Trifluoromethoxy)phenoxyaceticacidhydrazide|Pyrazine, 1,2-dihydro-2-imino-|2-aminopyrazin|pyrazin-2-amine|2 -aminopyrazine|4-Cyano-4-(3-methoxyphenyl)-1-methylpiperidine|(p-Cyanophenyl)acetic acid|Pyrazine amine|pyrazine-2-amine
Visão geral Aminopyrazine is a synthetic intermediate.
Especificações Sinónimos
Pyrazine, 2-amino- | pyrazineamine | 2-(1,3-dioxoisoindolin-2-yl)ethyl acetate | Aminopyrazine | amino-pyrazine | AMINO PYRAZINE | 1,2-Dihydro-2-iminopyrazine | 3-AMINOPYRAZINE | iminopyrazine | Octanoic acid, 2-methylpropyl ester | 2-Aminopyrazine | PYRIDINE,2-CHLORO-3-NITRO- | 2-Pyrazinamine | pyrazin-2-ylamine | Pyrazin-2-yl-amine | Py Show more
Especificações e pureza
≥99%
Condições de armazenamento de armazenamento
Room temperature
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488185616
Sorrisos canónicos
C1=CN=C(C=N1)N
IUPAC Name
pyrazin-2-amine
InChIKey
XFTQRUTUGRCSGO-UHFFFAOYSA-N
INCHI
1S/C4H5N3/c5-4-3-6-1-2-7-4/h1-3H,(H2,5,7)
SMILES isoméricas
C1=CN=C(C=N1)N
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107025&ln=
Dados avançados Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Classe Diazines Subclass Pyrazines Intermediate Tree Nodes Not available Direct Parent Aminopyrazines Alternative Parents Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Aminopyrazine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound Descrição This compound belongs to the class of organic compounds known as aminopyrazines. These are organic compounds containing an amino group attached to a pyrazine ring. 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.
Estrutura 3D Alvos associados (humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Solubilidade Soluble in water. Ponto de fusão (°C) 117-120°C Peso molecular 95.100 g/mol XLogP3 -0.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 0 Exact Mass 95.0483 Da Monoisotopic Mass 95.0483 Da Topological Polar Surface Area 51.800 Ų Heavy Atom Count 7 Formal Charge 0 Complexity 54.900 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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
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