C115002
Cyclopentylamine
99%
Synonym(s):
Aminocyclopentane
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About This Item
Linear Formula:
C5H9NH2
CAS Number:
Molecular Weight:
85.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-697-3
Beilstein/REAXYS Number:
635706
MDL number:
Assay:
99%
Form:
liquid
InChI key
NISGSNTVMOOSJQ-UHFFFAOYSA-N
InChI
1S/C5H11N/c6-5-3-1-2-4-5/h5H,1-4,6H2
SMILES string
NC1CCCC1
assay
99%
form
liquid
Quality Level
bp
106-108 °C (lit.)
density
0.863 g/mL at 25 °C (lit.)
Related Categories
General description
Cycloheptylamineis a versatile compound that has several useful applications in organicsynthesis. Its ability to act as a building block, catalyst, and reagent makesit a valuable tool for the development of new organic compounds. It is alsoused as a reagent for the functionalization of organic molecules.
Application
Cycloheptylamine is a building block for the formation of an ABX3-typed perovskite structure compound [C5H9–NH3][CdCl3].
signalword
Danger
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Skin Sens. 1
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
52.7 °F - closed cup
flash_point_c
11.5 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Room-temperature ABX 3-typed molecular ferroelectric:[C 5 H 9-NH 3][CdCl 3]
Zhang, Yi and Ye, et al.
Inorganic chemistry frontiers, 1, 118-123 (2014)
M S Sansom et al.
Protein engineering, 6(1), 65-74 (1993-01-01)
The influenza A M2 protein forms cation-selective ion channels which are blocked by the anti-influenza drug amantadine. A molecular model of the M2 channel is presented in which a bundle of four parallel M2 transbilayer helices surrounds a central ion-permeable
M J Comin et al.
Nucleosides & nucleotides, 18(10), 2219-2231 (2000-01-05)
Purine carbanucleosides built on a 6-oxabicyclo[3.1.0]hexane template were synthesized from readily available 2-cyclopentenone employing a Mitsunobu reaction to incorporate the base onto the carbocyclic ring. Both adenosine and guanosine analogues exhibited moderate antiviral activity.
D G Craciunescu et al.
In vivo (Athens, Greece), 1(4), 229-234 (1987-07-01)
Ten new Pt (II) complexes were synthesized and tested as potential antitumor drugs in vitro on KB human tumour cell line, and in vivo against four experimental tumour systems (P388, L1210, ADJ/PC6A and Yoshida sarcoma). The complexes contained two primary
Maris Vilums et al.
Journal of medicinal chemistry, 56(19), 7706-7714 (2013-09-14)
Preclinical models of inflammatory diseases (e.g., neuropathic pain, rheumatoid arthritis, and multiple sclerosis) have pointed to a critical role of the chemokine receptor 2 (CCR2) and chemokine ligand 2 (CCL2). However, one of the biggest problems of high-affinity inhibitors of
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