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Cycloheptanamine

Names

[ CAS No. ]:
5452-35-7

[ Name ]:
Cycloheptanamine

[Synonym ]:
CycloheptylaMine 25GR
1-Cycloheptanamine
cycloheptyl amine
cycroheptylamine
MFCD00004153
Cycloheptylamine
cycloheptaneamine
EINECS 226-693-1
AMINOCYCLOHEPTANE
Cycloheptanamine

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
163.4±8.0 °C at 760 mmHg

[ Melting Point ]:
-18°C

[ Molecular Formula ]:
C7H15N

[ Molecular Weight ]:
113.201

[ Flash Point ]:
42.2±0.0 °C

[ Exact Mass ]:
113.120445

[ PSA ]:
26.02000

[ LogP ]:
1.96

[ Vapour Pressure ]:
2.1±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.456

[ Storage condition ]:
Flammables area

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226-H315-H335

[ Precautionary Statements ]:
P261

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R10;R20;R37

[ Safety Phrases ]:
S23

[ RIDADR ]:
UN 2734 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2921300090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2921300090

[ Summary ]:
2921300090 other cyclanic, cyclenic or cyclotherpenic mono- or polyamines, and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Oxygen-18 studies on the oxidative deamination mechanism of alicyclic primary amines in rabbit liver microsomes.

Arch. Biochem. Biophys. 215(2) , 433-43, (1982)

Identification of a novel class of selective Tpl2 kinase inhibitors: 4-Alkylamino-[1,7]naphthyridine-3-carbonitriles.

Bioorg. Med. Chem. 15(19) , 6425-42, (2007)

We have previously reported the discovery and initial SAR of the [1,7]naphthyridine-3-carbonitriles and quinoline-3-carbonitriles as Tumor Progression Loci-2 (Tpl2) kinase inhibitors. In this paper, w...

Interaction of aminoadamantane derivatives with the influenza A virus M2 channel-docking using a pore blocking model.

Bioorg. Med. Chem. Lett. 20 , 4182-7, (2010)

Interaction of aminoadamantanes with the influenza A virus M2 proton channel was analyzed by docking simulations of a series of synthetic aminoadamantane derivatives, of differing binding affinity, in...


More Articles


Related Compounds