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5-Methoxy-2,3,3-trimethylindolenine is a chemical compound with the molecular formula C13H17NO and a molar mass of 203.28 g/mol. It is an indole alkaloid, a type of heterocyclic compound that contains a nitrogen atom in its ring structure. 5-Methoxy-2,3,3-trimethylindolenine is found in various natural sources, such as plants and fungi, and has been studied for its potential pharmacological properties, including its effects on the central nervous system and its potential as a psychoactive substance. Furthermore, 5-Methoxy-2,3,3-trimethylindolenine has been investigated for its potential as a precursor in the synthesis of other compounds.

41382-23-4

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41382-23-4 Usage

Uses

Used in Pharmaceutical Industry:
5-Methoxy-2,3,3-trimethylindolenine is used as a pharmacological agent for its potential effects on the central nervous system. Its study is focused on understanding its impact on neurological functions and exploring its potential as a psychoactive substance.
Used in Chemical Synthesis:
5-Methoxy-2,3,3-trimethylindolenine is used as a precursor in the synthesis of other compounds. Its unique structure and properties make it a valuable component in the creation of new chemical entities for various applications, including pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 41382-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41382-23:
(7*4)+(6*1)+(5*3)+(4*8)+(3*2)+(2*2)+(1*3)=94
94 % 10 = 4
So 41382-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-8-12(2,3)10-7-9(14-4)5-6-11(10)13-8/h5-8,13H,1-4H3

41382-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-2,3,3-trimethyl-1,2-dihydroindole

1.2 Other means of identification

Product number -
Other names 2,3,3-TRIMETHYL-5-METHOXYINDOLINE

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:41382-23-4 SDS

41382-23-4Downstream Products

41382-23-4Relevant academic research and scientific papers

Oxidative palladium(II)-catalyzed dehydrogenative C-H/C-H cross-coupling of 2,3-substituted indolines with arenes at the C7 position

Jiao, Lin-Yu,Oestreich, Martin

supporting information, p. 10845 - 10848 (2013/09/02)

Directed directing group: The C7 position of the indoline nucleus is difficult to address in C-H activation. An oxidative palladium(II) catalysis that allows for cross-dehydrogenative coupling in that position with activation of the C-H bond of the arene component is disclosed here. This C-H/C-H cross-coupling is applicable to various indolines acetylated at the nitrogen atom. Substitution at C2 is crucial for the C-H activation to occur at C7 (see scheme).

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