GRADE & PURITY ≥98%

Synonyms

AKOS000169258 | FT-0601664 | W-205579 | tert-butyl (piperidin-3-ylmethyl)carbamate | Z285919722 | tert-butyl (piperidin-3-yl)methylcarbamate | (+/-)-3-(Boc-aminomethyl)piperidine, >=98.0% (TLC) | EN300-55508 | FT-0660085 | (S)-N-Boc-1-(3-piperidyl)methana

Storage

Room temperature

Shipped In

Normal

Descripción general

Reagent for: Preparation of Tylophorine analogs Enzymatic acylation

Specifications

Sinónimos

AKOS000169258 | FT-0601664 | W-205579 | tert-butyl (piperidin-3-ylmethyl)carbamate | Z285919722 | tert-butyl (piperidin-3-yl)methylcarbamate | (+/-)-3-(Boc-aminomethyl)piperidine, >=98.0% (TLC) | EN300-55508 | FT-0660085 | (S)-N-Boc-1-(3-piperidyl)methana

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: CC(C)(C)OC(=O)NCC1CCCNC1
• IUPAC Name: tert-butyl N-(piperidin-3-ylmethyl)carbamate
• InChIKey: KHPQHXGYYXYTDN-UHFFFAOYSA-N
• INCHI: 1S/C11H22N2O2/c1-11(2,3)15-10(14)13-8-9-5-4-6-12-7-9/h9,12H,4-8H2,1-3H3,(H,13,14)
• Isómeros SMILES: CC(C)(C)OC(=O)NCC1CCCNC1
• WGK Alemania: 3
• Peso molecular: 214.3
• Beilstein: 7023640
• Reaxy-Rn: 7023643
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7023643&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Piperidines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Piperidines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Piperidines
• Alternative Parents: Carbamate esters Organic carbonic acids and derivatives Dialkylamines Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Piperidine - Carbamic acid ester - Carbonic acid derivative - Secondary aliphatic amine - Secondary amine - Azacycle - Organopnictogen compound - Amine - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.
• 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.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Pseudomonas aeruginosa (123386 Activities)

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

Mecanismos de acción

Propiedades químicas y físicas

• Punto de fusión (°C): 60-70°C
• Peso molecular: 214.300 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 214.168 Da
• Monoisotopic Mass: 214.168 Da
• Topological Polar Surface Area: 50.400 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 211.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1