跳转至内容
Merck
CN

138576

1-金刚烷胺

97%

别名:

1-氨基金刚烷

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式(希尔记法):
C10H17N
化学文摘社编号:
分子量:
151.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-201-2
Beilstein/REAXYS Number:
2204333
MDL number:
Assay:
97%
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


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

金刚烷胺,又称氨基金刚烷,是金刚烷某个甲基被氨基取代形成的衍生物。常作为起始材料用于多种有机反应,例如单体合成与一锅合成金刚烷肼。

Application

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。


Still not finding the right product?

Explore all of our products under 1-金刚烷胺


ppe

dust mask type N95 (US), Eyeshields, Gloves

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



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)
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
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.



全球贸易项目编号

货号GTIN
138576-500G04061833498651
138576-100G04061838732347
138576-25G04061838732354
138576-5G04061838732361