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4,6-DIMETHYLINDOLE, an indole derivative with the molecular formula C10H11N, is a chemical compound featuring two methyl groups at the 4 and 6 positions of the indole ring. It is recognized for its potential biological activities, such as anticancer, antioxidant, and anti-inflammatory properties, and is utilized as a building block in the synthesis of pharmaceuticals and organic compounds. Additionally, it serves as a dye intermediate and in the production of synthetic perfumes. However, due to its potential for skin and eye irritation and toxicity upon ingestion or inhalation, careful handling is advised.

75948-77-5

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75948-77-5 Usage

Uses

Used in Pharmaceutical Industry:
4,6-DIMETHYLINDOLE is used as a building block for the synthesis of various pharmaceuticals and organic compounds, leveraging its potential biological activities, including anticancer, antioxidant, and anti-inflammatory properties.
Used in Dye Industry:
4,6-DIMETHYLINDOLE is used as a dye intermediate, contributing to the production of various dyes due to its chemical structure and properties.
Used in Perfumery:
4,6-DIMETHYLINDOLE is utilized in the production of synthetic perfumes, where its unique chemical composition contributes to the creation of distinct fragrances.

Check Digit Verification of cas no

The CAS Registry Mumber 75948-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,4 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75948-77:
(7*7)+(6*5)+(5*9)+(4*4)+(3*8)+(2*7)+(1*7)=185
185 % 10 = 5
So 75948-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N/c1-7-5-8(2)9-3-4-11-10(9)6-7/h3-6,11H,1-2H3

75948-77-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethyl-1H-indole

1.2 Other means of identification

Product number -
Other names 4,6-Dimethyl-indol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75948-77-5 SDS

75948-77-5Relevant academic research and scientific papers

β-Amino alcohols from anilines and ethylene glycol through heterogeneous Borrowing Hydrogen reaction

Llabres-Campaner, Pedro J.,Ballesteros-Garrido, Rafael,Ballesteros, Rafael,Abarca, Belén

supporting information, p. 5552 - 5561 (2017/08/22)

Borrowing Hydrogen (BH), also called Hydrogen Autotransfer (HA), reaction with neat ethylene glycol represents a key step in the preparation of β-amino alcohols. However, due to the stability of ethylene glycol, mono-activation has rarely been achieved. Herein, a combination of Pd/C and ZnO is reported as heterogeneous catalyst for this BH/HA reaction. This system results in an extremely air and moisture stable, and economic catalyst able to mono-functionalize ethylene glycol in water, without further activation of the diol. In this work, different diols and aromatic amines have been explored affording a new approach towards amino alcohols. This study reveals how the combination of two solid species can afford interesting catalytic properties in heterogeneous phase. ZnO activates ethylene glycol while Pd/C is the responsible of the BH/HA cycle. This catalytic system has also been found useful to dehydrogenate indoles affording indolines that undergo in situ BH/HA cycle prior to re-aromatization, representing a tandem heterogeneous process.

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