29940
环丙胺
purum, ≥98.0% (GC)
别名:
氨基环丙烷
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关于此项目
线性分子式:
C3H5NH2
化学文摘社编号:
分子量:
57.09
EC Number:
212-142-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
741858
MDL number:
InChI key
HTJDQJBWANPRPF-UHFFFAOYSA-N
InChI
1S/C3H7N/c4-3-1-2-3/h3H,1-2,4H2
SMILES string
NC1CC1
vapor pressure
4.67 psi ( 20 °C)
grade
purum
assay
≥98.0% (GC)
autoignition temp.
527 °F
impurities
≤1% water
bp
49-50 °C (lit.)
density
0.824 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
33.8 °F - closed cup
flash_point_c
1 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
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Isabella Hyla-Kryspin et al.
Organic & biomolecular chemistry, 6(22), 4167-4175 (2008-10-31)
Fluorine substituents in organic molecules do dramatically influence the electronic structure of neighbouring functional groups and the conformation of molecules. Hence the presence of fluorine in a compound changes its chemical reactivity and biological activity. On the basis of MP2
Catherine A Faler et al.
Organic letters, 9(10), 1987-1990 (2007-04-24)
An intermolecular Ti(IV)-mediated cyclopropanation reaction has been used to synthesize substituted 2-phenylcyclopropylamines and constrained analogues of the neurotransmitters histamine and tryptamine. Many hydroxy- and methoxy-substituted phenylcyclopropylamines are known to inhibit monoamine oxidase and have been shown to mimic hallucinogens. These
Song Ye et al.
Bioorganic & medicinal chemistry, 13(7), 2489-2499 (2005-03-10)
A series of para-ring-substituted (E)- and (Z)-1-aryl-2-fluorocyclopropylamines were examined as inhibitors of recombinant human liver monoamine oxidase A (MAO A) and B (MAO B). Unlike the parent 1-phenylcyclopropylamine, which is a selective inhibitor of MAO B, both (E)- and (Z)-diastereomers
Christopher L Shaffer et al.
Journal of the American Chemical Society, 124(28), 8268-8274 (2002-07-11)
The role of single electron transfer (SET) in P450-catalyzed N-dealkylation reactions has been studied using the probe substrates N-cyclopropyl-N-methylaniline (2a) and N-(1'-methylcyclopropyl)-N-methylaniline (2b). In earlier work, we showed that SET oxidation of 2a by horseadish peroxidase leads exclusively to products
Grazia Chiellini et al.
Steroids, 77(3), 212-223 (2011-12-03)
Selective inhibitors of CYP24A1 represent an important synthetic target in a search for novel vitamin D compounds of therapeutic value. In the present work, we show the synthesis and biological properties of two novel side chain modified 2-methylene-19-nor-1,25(OH)(2)D(3) analogs, the
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