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340,000+ produtos de pesquisa · Triple ISO certified · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque 1-Aminocyclohexanecarboxylic acid - ≥98% , CAS No.2756-85-6
Disponível para encomenda
Synonyms
1-Aminocyclohexane-1-carboxylic acid|Lopac-A-162|2-aminocyclohexane-2-carboxylic acid|1-Aminocyclohexanecarboxylic acid|1-amino-cyclohexanecarboxylic acid|1-Amino-1-cyclohexanecarboxylic acid|1-amino-1-cyclohexane-carboxylic acid|aminocyclohexanecarboxylic acid|l-aminocyclohexane-1-carboxylic acid|1-Amino-cyclohexylcarboxylic acid|alpha-Aminocyclohexanecarboxylic acid|1-azanylcyclohexane-1-carboxylic acid|1-Amino-1-cyclohexanecarboxylicacid|1-Aminocyclohexanecarboxyic acid|.alpha.-Aminocyclohexanecarboxylic acid|1-Amino-1-cyclohexane carboxylic acid|Homocycloleucine|Cycloleucine Methyl Ester.HCl|1-Amino-cyclohexanecarboxylicacid|.alpha.-Aminocyclohexanecarboxylic aicd|Cyclohexanecarboxylic acid, 1-amino-
Storage
Desiccated,Room temperature
Especificações Sinónimos
1-Aminocyclohexane-1-carboxylic acid | Lopac-A-162 | 2-aminocyclohexane-2-carboxylic acid | 1-Aminocyclohexanecarboxylic acid | 1-amino-cyclohexanecarboxylic acid | 1-Amino-1-cyclohexanecarboxylic acid | 1-amino-1-cyclohexane-carboxylic acid | aminocyclohexanecarboxylic acid | l-aminocyclohexane-1-carboxylic acid | 1-Amino-cyclohexylcarbo Show more
Especificações e pureza
≥98%
Condições de armazenamento de armazenamento
Desiccated,Room temperature
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504750484
Sorrisos canónicos
C1CCC(CC1)(C(=O)O)N
IUPAC Name
1-aminocyclohexane-1-carboxylic acid
InChIKey
WOXWUZCRWJWTRT-UHFFFAOYSA-N
INCHI
1S/C7H13NO2/c8-7(6(9)10)4-2-1-3-5-7/h1-5,8H2,(H,9,10)
SMILES isoméricas
C1CCC(CC1)(C(=O)O)N
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2355692&ln=
Dados avançados Taxonomic Classification 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 D-alpha-amino acids Cyclohexylamines Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic homomonocyclic compounds Substituents D-alpha-amino acid - L-alpha-amino acid - Cyclohexylamine - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Aliphatic homomonocyclic compound Descrição 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 alpha-amino acid 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 Solubility in Water almost transparency Sensibilidade Hygroscopic. Ponto de fusão (°C) >300°C Peso molecular 143.180 g/mol XLogP3 -1.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 143.095 Da Monoisotopic Mass 143.095 Da Topological Polar Surface Area 63.300 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 139.000 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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