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C115002

Sigma-Aldrich

Cyclopentylamine

99%

Sinónimos:

Aminocyclopentane

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About This Item

Fórmula lineal:
C5H9NH2
Número de CAS:
1003-03-8
Peso molecular:
85.15
Beilstein/REAXYS Number:
635706
EC Number:
213-697-3
MDL number:
MFCD00001380
UNSPSC Code:
12352100
PubChem Substance ID:
24892364
NACRES:
NA.22

Quality Level

100

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

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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_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
STBJ8516
STBH7620
STBH1991
STBF1084V
S72096V

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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
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.
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
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

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