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488100

Sigma-Aldrich

Aniline-15N

98 atom % 15N

Synonym(s):

Benzenamine-15N

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About This Item

Linear Formula:
C6H515NH2
CAS Number:
7022-92-6
Molecular Weight:
94.12
MDL number:
MFCD00084195
UNSPSC Code:
12352116
PubChem Substance ID:
24872331
NACRES:
NA.12

isotopic purity

98 atom % 15N

Assay

99% (CP)

refractive index

n20/D 1.586 (lit.)

bp

184 °C (lit.)

mp

−6 °C (lit.)

density

1.033 g/mL at 25 °C

mass shift

M+1

storage temp.

2-8°C

SMILES string

[15NH2]c1ccccc1

InChI

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

InChI key

PAYRUJLWNCNPSJ-CDYZYAPPSA-N

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Packaging

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.

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

158.0 °F - closed cup

Flash Point(C)

70 °C - closed cup

Certificates of Analysis (COA)

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Conghui Tang et al.
Journal of the American Chemical Society, 134(46), 18924-18927 (2012-11-08)
A novel and efficient copper-catalyzed azidation reaction of anilines via C-H activation has been developed. This method, in which the primary amine acts as a directing group by coordinating to the metal center, provides ortho azidation products regioselectively under mild
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
Yu Qian et al.
Chemical communications (Cambridge, England), 49(26), 2700-2702 (2013-02-26)
An enantioselective four-component reaction of a diazoketone, water, an aniline and ethyl glyoxylate in the presence of catalytic Rh2(OAc)4 and a chiral Brønsted acid was developed to efficiently produce β-hydroxy-α-amino acid derivatives in good yields with high diastereoselectivity and enantioselectivity.
Ping-Xin Zhou et al.
Chemical communications (Cambridge, England), 49(6), 561-563 (2012-12-05)
Two different cyclic amino esters are synthesized by palladium-catalyzed cross-coupling reaction of diazoesters with N-substituted-2-iodoanilines. Aryldiazoacetates lead to cyclic α-amino esters with an α-quaternary carbon centre in the presence of CO. Additionally, arylvinyldiazoacetates afford cyclic α,β-unsaturated γ-amino esters.
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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