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1H-Indole-2-carboxamide, 4,5,6,7-tetrahydro-N,N-dimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89649-60-5

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89649-60-5 Usage

Molecular Structure

1H-Indole-2-carboxamide, 4,5,6,7-tetrahydro-N,N-dimethyl-3-phenylis a complex organic compound consisting of an indole ring fused with a pyrrolidine ring, a carboxamide group, and a phenyl ring connected through a methylene bridge.

Indole Derivative

The compound is derived from the indole structure, which is a bicyclic aromatic system with a benzene ring fused to a pyrrole ring.

Carboxamide Group

The molecule contains a 2-carboxamide group, which is an amide derivative of a carboxylic acid, providing potential sites for hydrogen bonding and interactions with biological targets.

Tetrahydro

The compound has a 4,5,6,7-tetrahydro structure, indicating that it has four additional hydrogen atoms in the core structure, making it more lipophilic and potentially more bioavailable.

N,N-Dimethyl

The molecule has two methyl groups attached to the nitrogen atom of the carboxamide group, increasing its molecular weight and potentially affecting its solubility and pharmacokinetic properties.

Pharmaceutical Potential

Due to its unique structure and the presence of various functional groups, 1H-Indole-2-carboxamide, 4,5,6,7-tetrahydro-N,N-dimethyl-3-phenylmay have potential applications in the pharmaceutical industry, possibly as a drug candidate or a precursor to other bioactive compounds.

Further Research

Despite its potential, more research and studies are needed to fully understand the properties, biological activity, and potential applications of 1H-Indole-2-carboxamide, 4,5,6,7-tetrahydro-N,N-dimethyl-3-phenyl-. This includes investigating its pharmacokinetics, pharmacodynamics, and toxicity profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 89649-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,4 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89649-60:
(7*8)+(6*9)+(5*6)+(4*4)+(3*9)+(2*6)+(1*0)=195
195 % 10 = 5
So 89649-60-5 is a valid CAS Registry Number.

89649-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-3-phenyl-4,5,6,7-tetrahydro-1H-indole-2-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Indole-2-carboxamide,4,5,6,7-tetrahydro-N,N-dimethyl-3-phenyl

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:89649-60-5 SDS

89649-60-5Downstream Products

89649-60-5Relevant academic research and scientific papers

The Synthesis and Chemistry of Azolenines. Part 2. A General Synthesis of Pyrrole-2-carboxylic Acid Derivatives by the Reaction of 2H-Azirines with Enamines, and the Crystal and Molecular Structure of Ethyl 3-Phenyl-4,5,6,7-tetrahydroindole-2-carboxylate

Law, Kam Wah,Lai, Ting-Fong,Sammes, Michael P.,Katritzky, Alan R.,Mak, Thomas C.W.

, p. 111 - 118 (2007/10/02)

A new general synthesis of 1H-pyrrole-2-carboxylic acid derivatives is described.Reaction between appropriately substituted 2H-azirines and enamines gives a mixture of 2,3- and 3,4-dihydropyrroles, which on acid treatment yields the title compounds in mod

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