274186
4-氨基苯甲酸甲酯
98%
别名:
4-(甲酯基)苯胺, 4-氨基苯甲酸甲酯, 对氨基苯甲酸甲酯, 对甲氧基苯胺, 甲基苯胺-4-羧酸酯, （4-（甲酯基）苯基）胺
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关于此项目
线性分子式:
H2NC6H4CO2CH3
化学文摘社编号:
分子量:
151.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-598-7
Beilstein/REAXYS Number:
775913
MDL number:
产品名称
4-氨基苯甲酸甲酯, 98%
InChI key
LZXXNPOYQCLXRS-UHFFFAOYSA-N
InChI
1S/C8H9NO2/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5H,9H2,1H3
SMILES string
COC(=O)c1ccc(N)cc1
assay
98%
form
solid
mp
110-111 °C (lit.)
functional group
ester
Quality Level
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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。
General description
研究了过氧化氢对 4-氨基苯甲酸甲酯的催化氧化。
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
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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
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[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
W Addicks et al.
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Stainless-steel templates of various thicknesses (75, 200, 800, and 1600 microns) were used to apply propylene glycol/water gels containing methyl or propyl p-aminobenzoates to silicone rubber membranes, and drug delivery was studied with the use of the Bronaugh diffusion cell
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