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
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.450 (lit.)
bp
106-108 °C (lit.)
density
0.863 g/mL at 25 °C (lit.)
SMILES string
NC1CCCC1
InChI
1S/C5H11N/c6-5-3-1-2-4-5/h5H,1-4,6H2
InChI key
NISGSNTVMOOSJQ-UHFFFAOYSA-N
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.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C115002-25G | 04061836830380 |
| C115002-100G | 04061838352941 |