
2-Methyl-4-nitroaniline | CAS:99-52-5
2-Methyl-4-nitroaniline
- 名称:4-硝基-2-甲苯胺 | 2-Methyl-4-nitroaniline
- CAS号:99-52-5
- 别名:2-Amino-5-nitrotoluene ; 4-Nitro-o-toluidine; Azoic Diazo No. 34; C.I. 37100
- 分子式:C7H8N2O2
- 分子量:152.15
- EINESC号:202-762-1
产品描述
物理化学性质
熔点 | 129-133 ºC |
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安全数据
危险品标志 | T;N |
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危险类别码 | R23/24/25;R33;R51/53 |
安全说明书 | S28A;S36/37;S45;S61 |
SDS
来源 | SDS样本 |
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没有数据 | 没有数据 |
产品合成路线
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同行评议文献
Highly diastereoselective alkylation of vicinal dianions of chiral succinic acid derivatives: a new general strategy to (R)-?-arylmethyl-?-butyrolactones.Pohmakotr M, et al. Tetrahedron Letters, 45(22), 4315-4318 (2004)
Sequential one-pot ruthenium-catalyzed azide-alkyne cycloaddition from primary alkyl halides and sodium azide.Johan R Johansson et al.The Journal of organic chemistry, 76(7), 2355-2359 (2011-03-11)
Mild conversion of beta-diketones and beta-ketoesters to carboxylic acids.Yang Zhang et al.The Journal of organic chemistry, 71(12), 4516-4520 (2006-06-06)
Marginally designed new profen analogues have the potential to inhibit cyclooxygenase enzymes.Hayrettin O Gülcan et al.Archiv der Pharmazie, 348(1), 55-61 (2015-01-13)
Synthesis of (-)-kainic acid using chiral lithium amides in an asymmetric dearomatizing cyclization.Clayden J, et al. Tetrahedron, 58(23), 4727-4733 (2002)
Application of sulfur ylide mediated epoxidations in the asymmetric synthesis of ?-hydroxy-d-lactones. Synthesis of a mevinic acid analogue and (+)-prelactone B.Aggarwal VK, et al. Tetrahedron Asymmetry, 60(43), 9725-9733 (2004)
Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.William L Scott et al.Journal of combinatorial chemistry, 11(1), 14-33 (2008-12-25)
备注
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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