114306-17-1

Basic information

• Product Name: 3-acetoxy-6-broMoindole
• Synonyms: 3-acetoxy-6-broMoindole;6-BroMo-1H-indol-3-yl acetate;1H-Indol-3-ol, 6-broMo-, 3-acetate
• CAS NO: 114306-17-1
• Molecular Formula: C₁₀H₈BrNO₂
• Molecular Weight: 254.08002
• Mol File: 114306-17-1.mol

Chemical Properties

• Boiling Point: 393.3±22.0 °C(Predicted)
• Appearance: /
• Density: 1.632±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.96±0.30(Predicted)
• CAS DataBase Reference: 3-acetoxy-6-broMoindole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-acetoxy-6-broMoindole(114306-17-1)
• EPA Substance Registry System: 3-acetoxy-6-broMoindole(114306-17-1)

Safety Data

• Hazardous Substances Data: 114306-17-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Acetoxy-6-bromoindole is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities, including its anti-inflammatory and anticancer properties. It plays a crucial role in the development of new drugs targeting inflammation and cancer.
Used in Agrochemical Industry:
3-Acetoxy-6-bromoindole is also utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products to protect crops and enhance yield.

Upstream product

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• 101861-53-4 2-(methylcarbonylamino)-4-bromobenzoic acid 
• 20776-50-5 2-amino-4-bromobenzoic acid 
• 116436-10-3 5’-bromo-2’-methylacetanilide 
• 244256-21-1 4-bromo-2-[(N-carboxymethyl)amino]benzoic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 19201-53-7 tyrian purple 
• 19201-53-7 6,6′?di?bromo?indigo 

Relevant articles and documents

Nanowires of indigo and isoindigo-based molecules with thermally removable groups

In this manuscript, indigo and isoindigo-based π-conjugated molecules with thermal removable tert-butoxycarbonyl (t-Boc) side groups were designed and synthesized. It was noted that the t-Boc side groups can be eliminated in nearly quantitative yields after thermal treatment at 200°C for 15 min, as confirmed by thermogravimetric analysis and Fourier transform infrared spectroscopy. From the thermal treated solution of isoindigo-based molecule DTIIC8C12 in the co-solvent of 1,2-dichlorobenzene/pyridine with volume ratio of 10/90, one-dimensional nanowires can be formed due to the hydrogen bonding assisted self-assembly. The afforded nanowires exhibited a moderate hole mobility of 1.3 × 10-3 cm2 V-1 s-1, as estimated from the organic field effect transistors. These observations illustrated that the utilization of thermal removable side chain functionalized conjugated polymers can be an effective strategy for developing conjugated polymers with impressive charge carrier transport.

Ambipolar organic phototransistors based on 6,6′-dibromoindigo

Ambipolar organic phototransistors were fabricated using a natural pigment 6,6′-dibromoindigo (6-BrIG) as the active channel. These phototransistors yielded significantly enhanced currents upon light illumination with photoresponsivities and external quantum efficiencies as high as 10.3 A W-1 and 2437% for the n-channel, and 55.4 mA W-1 and 13.1% for the p-channel, respectively. In addition, simple inverter complementary circuits were fabricated by integrating two ambipolar phototransistors. Channel current was dependent on light intensity and voltage bias. This study provides a basis for an in-depth understanding of the optoelectronic characteristics of 6-BrIG, and introduces this material as an ecofriendly candidate for optoelectronic applications.