产品名称

英文名称：1-Methyl-3-indoleacetic acid

同义词

1912-48-7、1-Methyl-3-indoleacetic acid、2-(1-methyl-1H-indol-3-yl)acetic acid、2-(1-methylindol-3-yl)acetic acid、1-methylindole-3-acetic acid、1h-indole-3-acetic acid, 1-methyl-、(1-methyl-1h-indol-3-yl)acetic acid、MFCD00130160、(1-methyl-3-indolyl)acetic acid

产品性质

CAS编号：1912-48-7

分子式：C11H11NO2

分子量：189.21

MDL号：MFCD00130160

PubChem编号：254166

英文别名：1912-48-7|1-Methyl-3-indoleacetic acid|2-(1-methyl-1H-indol-3-yl)acetic acid|2-(1-methylindol-3-yl)acetic acid|1-methylindole-3-acetic acid|1h-indole-3-acetic acid, 1-methyl-|(1-methyl-1h-indol-3-yl)acetic acid|MFCD00130160|(1-methyl-3-indolyl)acetic acid

规格或纯度：98%

英文名称：1-Methyl-3-indoleacetic acid

应用：·Reactant for enantioselective preparation of α-aryl alkylcarboxylic acids·Reactant for preparation of PKC inhibitor methylindolylpyridinylmet<WBR>hylpiperidinylindolylpyrr<WBR>oledione for protein kinase C imaging·Reactant for stereoselective preparation of δ-lactones via Michael addition/lactonization with unsaturated carboxylates·Reactant for stereoselective preparation of vindorosine, vindoline, and analogs·Reactant for preparation of (indolyl)pyrrol-2-ones as VEGF-R inhibitors, antiangiogenic agents, and protein kinase inhibitors·Reactant for synthesis of 3-aryl-5-alkyl-2,5-dihydr<WBR>ofuran-2-ones and their carbanalogues as antifungal agents.

运输条件：常规运输

产品介绍：·Reactant for enantioselective preparation of α-aryl alkylcarboxylic acids·Reactant for preparation of PKC inhibitor methylindolylpyridinylmethylpiperidinylindolylpyrroledione for protein kinase C imaging·Reactant for stereoselective preparation of δ-lactones via Michael addition/lactonization with unsaturated carboxylates·Reactant for stereoselective preparation of vindorosine, vindoline, and analogs·Reactant for preparation of (indolyl)pyrrol-2-ones as VEGF-R inhibitors, antiangiogenic agents, and protein kinase inhibitors·Reactant for synthesis of 3-aryl-5-alkyl-2,5-dihydrofuran-2-ones and their carbanalogues as antifungal agents.1-Methyl-3-indoleacetic acid is an indole derivative. Direct and riboflavin- or Rose-Bengal-sensitized photo-oxidation of 1-methyl-3-indoleacetic acid in aqueous buffer (pH 5 or pH 8) containing 10% methanol has been studied.·Reactant for enantioselective preparation of α-aryl alkylcarboxylic acids·Reactant for preparation of PKC inhibitor methylindolylpyridinylmethylpiperidinylindolylpyrroledione for protein kinase C imaging·Reactant for stereoselective preparation of δ-lactones via Michael addition/lactonization with unsaturated carboxylates·Reactant for stereoselective preparation of vindorosine, vindoline, and analogs·Reactant for preparation of (indolyl)pyrrol-2-ones as VEGF-R inhibitors, antiangiogenic agents, and protein kinase inhibitors·Reactant for synthesis of 3-aryl-5-alkyl-2,5-dihydrofuran-2-ones and their carbanalogues as antifungal agents.

PubChem SID：488189052

IUPAC Name：2-(1-methylindol-3-yl)acetic acid

INCHI：InChI=1S/C11H11NO2/c1-12-7-8(6-11(13)14)9-4-2-3-5-10(9)12/h2-5,7H,6H2,1H3,(H,13,14)

InChi Key：NAIPEFIYIQFVFC-UHFFFAOYSA-N

Canonical SMILES：CN1C=C(C2=CC=CC=C21)CC(=O)O

Isomeric SMILES：CN1C=C(C2=CC=CC=C21)CC(=O)O

WGK Germany：3

PubChem CID：254166

闪点(℃)：191 °C

沸点：392 °C

熔点：126-128 °C

象形图：

信号词：Danger

危险声明：H315 Causes skin irritationH335 May cause respiratory irritationH302 Harmful if swallowedH318 Causes serious eye damage

预防措施声明：P261,P280,P302+P352,P321,P405,P501,P264,P271,P270,P304+P340,P403+P233,P362+P364,P330,P264+P265,P301+P317,P305+P354+P338,P317,P332+P317,P319

产品包装