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C99604

Cycloheptylamine

99%

Synonym(s):

Aminocycloheptane

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About This Item

Linear Formula:
C7H13NH2
CAS Number:
5452-35-7
Molecular Weight:
113.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893208
EC Number:
226-693-1
Beilstein/REAXYS Number:
1847543
MDL number:
MFCD00004153
Assay:
99%
Form:
liquid
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Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.472 (lit.)

bp

54 °C/11 mmHg (lit.)

density

0.889 g/mL at 25 °C (lit.)

SMILES string

NC1CCCCCC1

InChI

1S/C7H15N/c8-7-5-3-1-2-4-6-7/h7H,1-6,8H2

InChI key

VXVVUHQULXCUPF-UHFFFAOYSA-N

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

107.6 °F

flash_point_c

42 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6731
STBK5954
STBB2739V
STBC5618V
STBC0558V

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Neelu Kaila et al.
Bioorganic & medicinal chemistry, 15(19), 6425-6442 (2007-08-01)
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, we report new SAR efforts which have led to the identification of 4-alkylamino-[1,7]naphthyridine-3-carbonitriles. These compounds show
Stelios Eleftheratos et al.
Bioorganic & medicinal chemistry letters, 20(14), 4182-4187 (2010-06-24)
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, into the crystal structure of the transmembrane (M2TM) pore. The pore blocking model
Julia Greiser et al.
Dalton transactions (Cambridge, England : 2003), 47(27), 9000-9007 (2018-06-21)
We report the isolation of a new type of 1,4-diazepan-6-amine (DAZA)-based ligand. Condensation of aldehydes with DAZA gives a novel class of 1,5-diazabicyclo[3.2.1]octanes in nearly quantitative yields. Subsequent reductive cleavage of these bicyclic aminal species with sodium borohydride selectively leads
View All Related Papers

Global Trade Item Number

SKUGTIN
C99604-25G04061833531402
C99604-100G04061838353382