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品質等級
化驗
97%
形狀
liquid
折射率
n20/D 1.612 (lit.)
bp
123-124 °C/10 mmHg (lit.)
mp
22 °C (lit.)
密度
1.075 g/mL at 25 °C (lit.)
SMILES 字串
CNc1ccccc1N
InChI
1S/C7H10N2/c1-9-7-5-3-2-4-6(7)8/h2-5,9H,8H2,1H3
InChI 密鑰
RPKCLSMBVQLWIN-UHFFFAOYSA-N
一般說明
N-甲基-1,2-苯二胺是一种 邻位 -二胺。N-甲基-1,2-苯二胺的原位生成重氮化阳离子曾用于玻碳电极的电化学修饰。
應用
N -甲基-1,2-苯二胺可用于以下研究:
- 一锅法合成 1-甲基-2-(杂)芳基苯并咪唑。
- 1-甲基-1 H -苯并咪唑-2(3 H )-硫酮的制备。
- 血管紧张素 II 受体拮抗剂替米沙坦的全合成。
- 烯酮二硫代缩醛制备苯并咪唑类。
訊號詞
Warning
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
235.4 °F - closed cup
閃點(°C)
113 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Synthesis, 1273-1273 (1992)
Beilstein journal of organic chemistry, 6, 25-25 (2010-05-27)
An efficient synthesis of the angiotensin II receptor antagonist Telmisartan (1) is presented involving a cross coupling of 4-formylphenylboronic acid 10 with 2-(2-bromophenyl)-4,4-dimethyl-2-oxazoline (11) as the key step (90% yield). The benzimidazole moiety 15 was constructed regioselectively via a reductive
Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis.
Journal of the Iranian Chemical Society, 6(1), 1-54 (2009)
Acta crystallographica. Section E, Structure reports online, 64(Pt 6), o1141-o1141 (2008-01-01)
The title compound, C(8)H(8)N(2)S, was prepared by the condensation of N-methyl-1,2-phenyl-enediamine and carbon disulfide. The crystal structure is stabilized by a C-H⋯π inter-action between a benzene H atom and the benzene ring of a neighbouring mol-ecule, and by inter-molecular N-H⋯S
Langmuir : the ACS journal of surfaces and colloids, 24(16), 8711-8718 (2008-07-26)
The electrochemically induced functionalization of glassy carbon electrode by aryl groups having an aliphatic amine group was achieved by reduction of in situ generated diazonium cations in aqueous media. The corresponding diazonium cations of 4-aminobenzylamine, 2-aminobenzylamine, 4-(2-aminoethyl)aniline, N-methyl-1,2-phenylenediamine, and N
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