586765
苯胺-4-13C
99 atom % 13C
别名:
Benzenamine-4-13C
同位素纯度
99 atom % 13C
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
Nc1cc[13cH]cc1
InChI
1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i1+1
InChI key
PAYRUJLWNCNPSJ-OUBTZVSYSA-N
一般描述
Aniline-4-13C 99 atom % 13C is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.
应用
- High-resolution NMR spectroscopy
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- reaction mechanism investigations
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- reaction mechanism investigations
特点和优势
Features
Benefits
- Cutting-edge technology in production.
- Comprehensive support and documentation provided.
- Flexible ordering options for different scales.
- Expert technical assistance available.
Benefits
- Streamlines the synthesis of complex molecules.
- Supports innovative approaches in organic chemistry.
- Enhances the efficiency of chemical reactions.
- Facilitates the development of new therapeutic agents.
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)
168.8 °F - closed cup
闪点(°C)
76 °C - closed cup
Ronald Besandre et al.
Organic letters, 15(7), 1666-1669 (2013-03-15)
N-substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an α-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those
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
Roman Spesyvtsev et al.
Faraday discussions, 157, 165-179 (2012-12-13)
Femtosecond time-resolved photoelectron imaging is employed to investigate ultrafast electronic relaxation in aniline, a prototypical aromatic amine. The molecule is excited at wavelengths between 269 and 238 nm. We observe that the S2(pi3s/pi sigma*) state is populated directly during the
Chia-Chi Su et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(9), 1012-1018 (2013-04-12)
This study was undertaken to investigate the feasibility of applying the Fered-Fenton process to the degradation of m-phenylenediamine, by examining the effect of varying the initial H2O2 and Fe(2+) concentrations, the initial pH and electric current on the process efficiency.
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.
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