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138576

Sigma-Aldrich

1-Adamantylamine

97%

Synonym(s):

1-Aminoadamantane

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About This Item

Empirical Formula (Hill Notation):
C10H17N
CAS Number:
768-94-5
Molecular Weight:
151.25
Beilstein:
2204333
EC Number:
212-201-2
MDL number:
MFCD00074732
UNSPSC Code:
12352100
PubChem Substance ID:
24848359
NACRES:
NA.22

Quality Level

200

Assay

97%

mp

206-208 °C (lit.)

solubility

1 M HCl: soluble 5%, clear to hazy, colorless to faint yellow or tan

SMILES string

NC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2/t7-,8+,9-,10-

InChI key

DKNWSYNQZKUICI-CHIWXEEVSA-N

Gene Information

human ... GRIN2A(2903)

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Application

1-Adamantylaminecan be used as a reactant to synthesize:
  • Adamantyl ureas by reacting with isocyanates in the presence of triethylamine.
  • N-(1-adamantyl)-2-chloroacetamide from chloroacetyl chloride in the presence of potassium carbonate.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

8.18383

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A series of novel 1,2,3-triazole-adamantylacetamide hybrids 5a-u, designed by combining bioactive fragments from antitubercular I-A09 and substituted adamantyl urea, were synthesized using copper catalyzed click chemistry. N-(1-Adamantyl)-2-azido acetamide 3 prepared from 1-adamantylamine was reacted with a series of alkyl/aryl acetylenes
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