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Merck
CN

488100

Sigma-Aldrich

苯胺-15N

98 atom % 15N

别名:

Benzenamine-15N

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About This Item

线性分子式:
C6H515NH2
CAS号:
分子量:
94.12
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.12

同位素纯度

98 atom % 15N

质量水平

方案

99% (CP)

折射率

n20/D 1.586 (lit.)

沸点

184 °C (lit.)

mp

−6 °C (lit.)

密度

1.033 g/mL at 25 °C

质量偏移

M+1

储存温度

2-8°C

SMILES字符串

[15NH2]c1ccccc1

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i7+1

InChI key

PAYRUJLWNCNPSJ-CDYZYAPPSA-N

包装

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Resp. Sens. 1

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

158.0 °F - closed cup

闪点(°C)

70 °C - closed cup

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Chemical communications (Cambridge, England), 49(2), 173-175 (2012-11-22)
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Timo Stahl et al.
Journal of the American Chemical Society, 135(4), 1248-1251 (2013-01-15)
Heterolytic splitting of the Si-H bond mediated by a Ru-S bond forms a sulfur-stabilized silicon cation that is sufficiently electrophilic to abstract fluoride from CF(3) groups attached to selected anilines. The ability of the Ru-H complex, generated in the cooperative
Sung Jin Bae et al.
European journal of medicinal chemistry, 57, 383-390 (2012-11-15)
We attempted to design and synthesize (E)-N-substituted benzylidene-hydroxy or methoxy-aniline derivatives and to evaluate their inhibitory effect on tyrosinase activity and anti-melanogenesis activity in murine B16F10 melanoma cells. Derivatives with a 4-methoxy- or 4-hydroxy-anilino group exerted more potent inhibition against
Tommy Kenny et al.
Inorganic chemistry, 51(24), 13081-13095 (2012-11-23)
This work represents an effort to synthesize all four forms of polyaniline (PANI) in its organometallic versions. Polymers containing substituted 1,4-benzoquinone diimine or 1,4-diaminobenzene units in the backbone exhibiting the general structure (C≡CC(6)H(4)-N═C(6)X(4)═N-C(6)H(4)C≡C-PtL(2))(n) and (C≡CC(6)H(4)NH-C(6)X(4)-NHC(6)H(4)C≡C-PtL(2))(n) along with the corresponding model

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