138576
1-Adamantylamine
97%
Synonym(s):
1-Aminoadamantane
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C10H17N
CAS Number:
Molecular Weight:
151.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-201-2
Beilstein/REAXYS Number:
2204333
MDL number:
Assay:
97%
Quality Level
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)
General description
1-Adamantylamine, also known as Amantadine, is an adamantane derivative where an amino group is replaced by one of the methyl groups of adamantane. It is commonly used as a starting material in various organic reaction, such as monomer synthesis and one-pot synthesis of 1-adamantylhydrazine.
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.
Still not finding the right product?
Explore all of our products under 1-Adamantylamine
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Dinesh Addla et al.
Bioorganic & medicinal chemistry letters, 24(8), 1974-1979 (2014-04-01)
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
Márió Gajdács et al.
Antibiotics (Basel, Switzerland), 8(4) (2019-12-22)
Background: The emergence of multidrug-resistant organisms (MDROs) is a global public health issue, severely hindering clinicians in administering appropriate antimicrobial therapy. Drug repurposing is a drug development strategy, during which new pharmacological applications are identified for already approved drugs. From
Zari Hooshyar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 144-150 (2016-09-18)
In this study, we describe the synthesis of a new quantum dots (QDs) by embedding glutathione capped CdTe/ZnS QDs into cationic starch biopolymer (CS-GSH-CdTe/ZnS QDs). The fluorescence intensity of prepared QDs was significantly enhanced. When QDs interacted with rifampicin, the