Catalog No.:AA0025DE

17768-41-1 | 1-Adamantanemethylamine

Name: Name:1-Adamantanemethylamine
Brand: AABLOCKS
SKU: AA0025DE
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Rating: 90 (10 reviews)

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25g

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0025DE

Chemical Name:

1-Adamantanemethylamine

CAS Number:

17768-41-1

Molecular Formula:

C11H19N

Molecular Weight:

165.2753

MDL Number:

MFCD00074750

SMILES:

NCC12CC3CC(C2)CC(C1)C3

NSC Number:

285231

Properties

BP:

229.4°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.5137(lit.)

Stability:

Air Sensitive

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

156

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

2.2

Downstream Synthesis Route

23074-42-2

17768-41-1

[1]ChemicalScience,2018,vol.9,p.8553-8560

[2]OrganicLetters,2014,vol.16,p.1092-1095

[3]CanadianJournalofChemistry,1978,vol.56,p.2731-2736

[4]PharmaceuticalChemistryJournal,1987,vol.21,p.287-291 Khimiko-FarmatsevticheskiiZhurnal,1987,vol.21,p.454-458

[5]Chemistry-AEuropeanJournal,2013,vol.19,p.4437-4440

[6]Chemistry-AEuropeanJournal,2014,vol.20,p.4227-4231

[7]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.5944-5948

[8]Catalysisscienceandtechnology,2016,vol.6,p.4768-4772

[9]ChemCatChem,2016,vol.8,p.1329-1334

[10]AdvancedSynthesisandCatalysis,2016,vol.358,p.2163-2171

[11]ChemSusChem,2017,vol.10,p.842-846

[12]OrganicLetters,2017,vol.19,p.50-53

[13]ChemPlusChem,2019,vol.84,p.1508-1511

5511-18-2

17768-41-1

[1]Patent:WO2017/27984,2017,A1.Locationinpatent:Page/Pagecolumn33;34;39;40

[2]ACSChemicalNeuroscience,2014,vol.5,p.335-339

[3]Patent:WO2006/90244,2006,A1.Locationinpatent:Page/Pagecolumn28

[4]JournaloftheAmericanChemicalSociety,1985,vol.107,p.5717-5722

[5]Chemistry-AEuropeanJournal,2016,vol.22,p.5156-5159

[6]Patent:WO2008/64432,2008,A1.Locationinpatent:Page/Pagecolumn57;61

[7]BioorganicandMedicinalChemistryLetters,2014,vol.24,p.828-830

[8]Patent:WO2008/106128,2008,A2.Locationinpatent:Page/Pagecolumn28

[9]ChemischeBerichte,1963,vol.96,p.550-555

[10]ChemicalCommunications,1998,p.2297-2298

[11]PharmaceuticalChemistryJournal,1987,vol.21,p.287-291 Khimiko-FarmatsevticheskiiZhurnal,1987,vol.21,p.454-458

[12]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.3720-3723

[13]AngewandteChemie-InternationalEdition,2012,vol.51,p.1662-1666

[14]Molecules,2018,vol.23

[15]Tetrahedron,2018,vol.74,p.1207-1219

17768-41-1

14504-80-4

[1]JournaloftheAmericanChemicalSociety,1985,vol.107,p.5717-5722

[2]ChemischeBerichte,1963,vol.96,p.550-555

[3]ChemischeBerichte,1974,vol.107,p.1245-1256

17768-41-1

768-91-2

[1]JournalofOrganicChemistry,1984,vol.49,p.2875-2880

17768-41-1

13200-85-6

(S)-N-Adamantan-1-ylmethyl-2-formylamino-3-phenyl-propionamide

[1]Eblinger,Frank;Schneider,Hans-Joerg[ChemicalCommunications,1998,#21,p.2297-2298]

Literature

Title: An extended cavitand with an introverted carboxylic acid.

Journal: Chemical communications (Cambridge, England) 20100414

Title: cis-Bis[(1-adamantylmeth-yl)amine-κN]-dichloridoplatinum(II) N,N-dimethyl-formamide solvate.

Journal: Acta crystallographica. Section E, Structure reports online 20091101

Title: Simultaneous liquid chromatographic assay of amantadine and its four related compounds in phosphate-buffered saline using 4-fluoro-7-nitro-2,1,3-benzoxadiazole as a fluorescent derivatization reagent.

Journal: Biomedical chromatography : BMC 20060501

Title: Antiviral agents. 2. Structure-activity relationships of compounds related to 1-adamantanamine.

Journal: Journal of medicinal chemistry 19710601

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SDS