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124192-86-5

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124192-86-5 Usage

Description

(S)-N-Methyl-N-(2-propynyl)-2,3-dihydroinden-1-aMine, with the molecular formula C13H15N, is an amine compound characterized by the presence of a methyl group and a propynyl group attached to the nitrogen atom, and a dihydroindenyl group attached to the carbon atom. This organic compound is known for its potential applications in various fields, including organic synthesis, pharmaceutical research, and the development of new medications.

Uses

Used in Pharmaceutical Research:
(S)-N-Methyl-N-(2-propynyl)-2,3-dihydroinden-1-aMine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new medications with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-N-Methyl-N-(2-propynyl)-2,3-dihydroinden-1-aMine serves as a valuable building block for the creation of complex organic molecules. Its versatile structure enables the formation of a wide range of chemical compounds.
Used in the Production of Fine Chemicals and Specialty Materials:
(S)-N-Methyl-N-(2-propynyl)-2,3-dihydroinden-1-aMine is also utilized in the production of fine chemicals and specialty materials, where its unique properties can be harnessed to create high-value products with specific applications.
Used in the Development of Novel Chemical Compounds:
Due to its potential biological activities, (S)-N-Methyl-N-(2-propynyl)-2,3-dihydroinden-1-aMine may be used as a starting point for the development of novel chemical compounds with various applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 124192-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,9 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124192-86:
(8*1)+(7*2)+(6*4)+(5*1)+(4*9)+(3*2)+(2*8)+(1*6)=115
115 % 10 = 5
So 124192-86-5 is a valid CAS Registry Number.

124192-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-N-Methyl-N-(2-propyn-1-yl)-1-indanamine

1.2 Other means of identification

Product number -
Other names -

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:124192-86-5 SDS

124192-86-5Downstream Products

124192-86-5Relevant articles and documents

Methylation method of amines

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Paragraph 0109; 0110; 0111; 0112; 0113; 0114, (2017/12/04)

The invention provides a methylation method of amines. The method is characterized by comprising the steps that under the protection of nitrogen or inert gas, organic amines, a reductive agent polymethyl hydrogen siloxane or diphenyl silane, a catalyst potassium phosphate and an additive 18-crown-6 are added into a reaction container, and an reaction is made with carbon dioxide as a C1 source to obtain methylated products of amines. According to the method, potassium phosphate serves as the catalyst, the carbon dioxide serves as the C1 source, polymethyl hydrogen siloxane or diphenyl silane serves as the reductive agent, and 18-crown-6 serves as the additive. Various kinds of amines are converted into the corresponding methylated products in an acetonitrile solvent or without solvents. Two waste materials including the carbon dioxide and polymethyl hydrogen siloxane (PMHS) serve as the C1 source and the reductive agent in the method respectively, phosphate serves as the catalyst, the cost is low, and the conversion efficiency is high. Thus, the method makes an important contribution to the development of green chemistry.

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