914348-96-2

Basic information

• Product Name: 1-Boc-7-methyl-3-formylindole
• Synonyms: 1-Boc-7-methyl-3-formylindole;tert-Butyl 3-forMyl-7-Methyl-1H-indole-1-carboxylate;1H-INDOLE-1-CARBOXYLIC ACID, 3-FORMYL-7-METHYL-, 1,1-DIMETHYLETHYL ESTER;7-Methylindole-3-carboxaldehyde,N-BOCprotected98%
• CAS NO: 914348-96-2
• Molecular Formula: C₁₅H₁₇NO₃
• Molecular Weight: 259.303
• EINECS: 604-604-1
• Mol File: 914348-96-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 396.1°C at 760 mmHg
• Flash Point: 193.3°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 1.75E-06mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 1-Boc-7-methyl-3-formylindole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Boc-7-methyl-3-formylindole(914348-96-2)
• EPA Substance Registry System: 1-Boc-7-methyl-3-formylindole(914348-96-2)

Safety Data

• Hazardous Substances Data: 914348-96-2(Hazardous Substances Data)

Usage

General Description

1-Boc-7-methyl-3-formylindole is a chemical compound with the molecular formula C16H19NO2. It is a derivative of indole, a heterocyclic aromatic organic compound, and it contains a 1-Boc (tert-butoxycarbonyl) protecting group, a methyl group and a formyl group attached to the indole ring. 1-Boc-7-methyl-3-formylindole has potential applications in synthetic organic chemistry as a building block for the synthesis of various indole derivatives and pharmaceutical compounds. It may also be used in research and development of new drugs and agrochemicals. Its properties and potential reactivity make it an interesting molecule for further exploration in various fields of chemical science.

InChI:InChI=1/C15H17NO3/c1-10-6-5-7-12-11(9-17)8-16(13(10)12)14(18)19-15(2,3)4/h5-9H,1-4H3

Upstream product

• 4771-50-0 7-methyl-1H-indole-3-carbaldehyde 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1428969-84-9 2-((3-methoxyphenyl)amino)-1-(7-methyl-1H-indol-3-yl)-2-phenylethanone 

Relevant articles and documents

Structure-guided design, synthesis, and biological evaluation of (2-(1 H-Indol-3-yl)-1 H-imidazol-4-yl)(3,4,5-trimethoxyphenyl) methanone (ABI-231) analogues targeting the colchicine binding site in Tubulin

ABI-231 is a potent, orally bioavailable tubulin inhibitor that interacts with the colchicine binding site and is currently undergoing clinical trials for prostate cancer. Guided by the crystal structure of ABI-231 in complex with tubulin, we performed structure-activity relationship studies around the 3-indole moiety that led to the discovery of several potent ABI-231 analogues, most notably 10ab and 10bb. The crystal structures of 10ab and 10bb in complex with tubulin confirmed their improved molecular interactions to the colchicine site. In vitro, biological studies showed that new ABI-231 analogues disrupt tubulin polymerization, promote microtubule fragmentation, and inhibit cancer cell migration. In vivo, analogue 10bb not only significantly inhibits primary tumor growth and decreases tumor metastasis in melanoma xenograft models but also shows a significant ability to overcome paclitaxel resistance in a taxane-resistant PC-3/TxR model. In addition, pharmacological screening suggested that 10bb has a low risk of potential off-target function.