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Merck
CN

138576

Sigma-Aldrich

1-金刚烷胺

97%

别名:

1-氨基金刚烷

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About This Item

经验公式(希尔记法):
C10H17N
CAS号:
分子量:
151.25
Beilstein:
2204333
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

206-208 °C (lit.)

溶解性

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

SMILES字符串

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

基因信息

human ... GRIN2A(2903)

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一般描述

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.

应用

1-金刚烷胺可作为一种反应物,用于合成:
  • 在三乙胺存在下,与异氰酸酯反应可以制备1-金刚烷基脲。
  • 在碳酸钾存在下,与氯乙酰氯反应可以制备N-(1-金刚烷基)-2-氯乙酰胺。

象形图

Exclamation mark

警示用语:

Warning

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Terminal Modification with 1-Adamantylamine to Endow Hyperbranched Polyamidoamine with Thermo-/pH-Responsive Properties.
Guo Z, et al.
Macromolecular Rapid Communications, 29(21), 1746-1751 (2008)
Jinglun Huang et al.
The Journal of organic chemistry, 72(1), 204-208 (2006-12-30)
The enantioselective Strecker reaction of N-diphenylphosphinoyl ketoimines has been achieved by use of in situ prepared chiral N,N'-dioxide catalyst from l-piperidinamide 3f and m-chloroperoxybenzoic acid (m-CPBA). Excellent yields (up to 99%) and high enantioselectivities (up to 92% ee) were obtained.
Lei Deng et al.
Nature communications, 9(1), 359-359 (2018-01-26)
Current influenza vaccines provide limited protection against circulating influenza A viruses. A universal influenza vaccine will eliminate the intrinsic limitations of the seasonal flu vaccines. Here we report methodology to generate double-layered protein nanoparticles as a universal influenza vaccine. Layered
Uday K Sukumar et al.
Biomaterials, 218, 119342-119342 (2019-07-22)
The prognosis for glioblastoma (GBM) remains depressingly low. The biological barriers of the brain present a major challenge to achieving adequate drug concentrations for GBM therapy. To address this, we explore the potential of the nose-to-brain direct transport pathway to
Debajit Dey et al.
PLoS neglected tropical diseases, 13(7), e0007548-e0007548 (2019-07-25)
Viroporins like influenza A virus M2, hepatitis C virus p7, HIV-1 Vpu and picornavirus 2B associate with host membranes, and create hydrophilic corridors, which are critical for viral entry, replication and egress. The 6K proteins from alphaviruses are conjectured to

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