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488100

Sigma-Aldrich

Aniline-15N

98 atom % 15N

Synonyme(s) :

Benzenamine-15N

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About This Item

Formule linéaire :
C6H515NH2
Numéro CAS:
7022-92-6
Poids moléculaire :
94.12
Numéro MDL:
MFCD00084195
Code UNSPSC :
12352116
ID de substance PubChem :
24872331
Nomenclature NACRES :
NA.12

Pureté isotopique

98 atom % 15N

Niveau de qualité

200

Pureté

99% (CP)

Indice de réfraction

n20/D 1.586 (lit.)

Point d'ébullition

184 °C (lit.)

Pf

−6 °C (lit.)

Densité

1.033 g/mL at 25 °C

Changement de masse

M+1

Température de stockage

2-8°C

Chaîne SMILES 

[15NH2]c1ccccc1

InChI

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

Clé InChI

PAYRUJLWNCNPSJ-CDYZYAPPSA-N

Catégories apparentées

Conditionnement

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.

Mention d'avertissement

Danger

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

158.0 °F - closed cup

Point d'éclair (°C)

70 °C - closed cup

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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
A Subashini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 403-408 (2013-01-01)
One of the Schiff base 4-bromo-4'dimethylamino benzylideneaniline (BDMABA) compounds was synthesized and single crystal of the material was grown by solvent evaporation method at room temperature. Molecular structure of BDMABA was confirmed by (1)H nuclear magnetic resonance and the presence
Wen Chen et al.
Journal of the American Chemical Society, 135(11), 4438-4449 (2013-03-02)
A series of linear and cyclic, sequence controlled, DNA-conjoined copolymers of aniline (ANi) and 2,5-bis(2-thienyl)pyrrole (SNS) were synthesized. In one approach, linear copolymers were prepared from complementary DNA oligomers containing covalently attached SNS and ANi monomers. Hybridization of the oligomers
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
Dongdong Liang et al.
Chemical communications (Cambridge, England), 49(2), 173-175 (2012-11-22)
An efficient synthesis of free (NH)-phenanthridinones through Pd-catalyzed C(sp(2))-H aminocarbonylation of unprotected o-arylanilines under an atmospheric pressure of CO has been developed. Some ortho heteroarene substituted anilines as well as N-alkyl protected o-arylanilines are also suitable substrates for this C-H
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