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Benzenemethanamine, α,2,4,6-tetramethyl-, (αS)is an organic compound characterized by a complex structure. It features an amine group attached to a methylene group, which is directly connected to a benzene ring. The (αS)configuration indicates that it is a stereochemical enantiomer, meaning it is a non-superimposable mirror image of its other configuration. This chemical is composed of four methyl groups and exhibits reactivity with other chemicals, making it a versatile compound with potential applications in various scientific fields such as molecular biology, biochemistry, and synthetic organic chemistry. However, due to its potential risks, it should be handled with caution.

20050-17-3

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20050-17-3 Usage

Uses

Used in Molecular Biology:
Benzenemethanamine, α,2,4,6-tetramethyl-, (αS)is used as a reagent for the synthesis of various biologically active molecules, contributing to the development of new drugs and therapeutic agents.
Used in Biochemistry:
Benzenemethanamine, α,2,4,6-tetramethyl-, (αS)is employed as a building block in the synthesis of complex biomolecules, facilitating research in the field of biochemistry and understanding the structure and function of biological systems.
Used in Synthetic Organic Chemistry:
Benzenemethanamine, α,2,4,6-tetramethyl-, (αS)is used as an intermediate in the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals, due to its reactive nature and structural versatility.

Check Digit Verification of cas no

The CAS Registry Mumber 20050-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,5 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20050-17:
(7*2)+(6*0)+(5*0)+(4*5)+(3*0)+(2*1)+(1*7)=43
43 % 10 = 3
So 20050-17-3 is a valid CAS Registry Number.

20050-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzenemethanamine, α,2,4,6-tetramethyl-, (αS)-

1.2 Other means of identification

Product number -
Other names GDC-0349||GDC0349

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:20050-17-3 SDS

20050-17-3Downstream Products

20050-17-3Relevant academic research and scientific papers

A new non-natural chiral auxiliary: Design, synthesis, and resolution of 1-mesitylethylamine and its application in the asymmetric aza-Diels-Alder reaction

Kohara, Takehiro,Hashimoto, Yukihiko,Shioya, Rieko,Saigo, Kazuhiko

, p. 4831 - 4840 (2007/10/03)

1-Mesitylethylamine was designed as a new non-natural chiral auxiliary. Racemic 1-mesitylethylamine could be synthesized in two steps from mesityl cyanide and could be resolved via separation of diastereomeric carbamates derived from (-)-menthyl chlorofor

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