Quality Level
assay
98%
form
solid
mp
110-111 °C (lit.)
functional group
ester
SMILES string
COC(=O)c1ccc(N)cc1
InChI
1S/C8H9NO2/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5H,9H2,1H3
InChI key
LZXXNPOYQCLXRS-UHFFFAOYSA-N
General description
研究了过氧化氢对 4-氨基苯甲酸甲酯的催化氧化。
Application
4-氨基苯甲酸甲酯用于通过质子酸催化的杂 Diels-Alder 与 N-Cbz 2-吡咯啉的偶联反应合成胍生物碱、(±)-马二碱和(±)-马来酸。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Wipapan Pongcharoen et al.
Chemical & pharmaceutical bulletin, 55(11), 1647-1648 (2007-11-06)
Chemical investigation of the wood-decayed fungus Xylaria sp. BCC 9653 has led to the isolation of a new methyl aminobenzoate (1) together with eleven known compounds. The structures were established by analysis of spectroscopic data. Cytochalasin D (2), one of
Beate Priewisch et al.
The Journal of organic chemistry, 70(6), 2350-2352 (2005-03-12)
[reaction: see text] Reaction conditions are described for the oxidation of anilines furnishing nitrosoarenes and the synthesis of unsymmetrically substituted azobenzenes. In a comparative study, the catalytic oxidation of methyl 4-aminobenzoate by hydrogen peroxide was investigated, and SeO(2) proved to
David A Powell et al.
Organic letters, 4(17), 2913-2916 (2002-08-17)
[reaction: see text] A concise synthesis of the guanidine alkaloids, (+/-)-martinelline and (+/-)-martinellic acid, using a protic acid catalyzed 2:1 hetero Diels-Alder coupling reaction between N-Cbz 2-pyrroline and methyl 4-aminobenzoate, is described. Protic acid catalysis, rather than Lewis acid catalysis
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 483761-1G | 04061832390178 |
| 274186-25G | 04061826151877 |
| 274186-100G | 04061838348340 |
| 274186-5G | 04061826151884 |