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
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
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...