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601487-88-1

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601487-88-1 Usage

Description

Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorois a chemical compound with a unique molecular structure that features a trifluoroacetamide group attached to a 5-ethyl-2,3-dihydro-1H-inden-2-yl moiety. Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorois characterized by its potential reactivity and versatility in organic synthesis, making it a valuable component in the development of various chemical products.

Uses

Used in Organic Synthesis:
Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorois used as a reagent in organic synthesis for its ability to participate in a range of chemical reactions. Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoro-'s structure allows it to act as a building block or a modifying agent in the creation of more complex molecules, which can be utilized in various industries such as pharmaceuticals, materials science, and agrochemicals.
In the Pharmaceutical Industry:
Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorois used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be exploited to design and develop new drugs with specific therapeutic properties, potentially leading to the creation of novel treatments for various diseases and medical conditions.
In the Materials Science Industry:
Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorocan be used as a component in the development of advanced materials with specific properties, such as high thermal stability, chemical resistance, or unique mechanical characteristics. These materials can find applications in various fields, including electronics, aerospace, and automotive industries.
In the Agrochemical Industry:
Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorocan be employed in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness, selectivity, or environmental compatibility, contributing to more sustainable agricultural practices.
Overall, Acetamide, N-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluorois a versatile chemical compound with a wide range of potential applications across different industries, primarily due to its utility in organic synthesis and its unique molecular structure.

Check Digit Verification of cas no

The CAS Registry Mumber 601487-88-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,1,4,8 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 601487-88:
(8*6)+(7*0)+(6*1)+(5*4)+(4*8)+(3*7)+(2*8)+(1*8)=151
151 % 10 = 1
So 601487-88-1 is a valid CAS Registry Number.

601487-88-1SDS

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-(5-ethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide

1.2 Other means of identification

Product number -
Other names ACETAMIDE,N-(5-ETHYL-2,3-DIHYDRO-1H-INDEN-2-YL)-2,2,2-TRIFLUORO

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:601487-88-1 SDS

601487-88-1Relevant articles and documents

An efficient and economical synthesis of 5,6-diethyl-2,3-dihydro-1H-inden- 2-amine hydrochloride

Prashad, Mahavir,Hu, Bin,Har, Denis,Repic, Oljan,Blacklock, Thomas J.,Lohse, Olivier

, p. 135 - 141 (2012/12/21)

An efficient and economical synthesis of 5,6-diethyl-2,3-dihydro-1H-inden- 2-amine hydrochloride (1) utilizing 2-aminoindan as a cheap and commercially readily available starting material is described. The newly developed synthesis involves six-steps with 49% overall yield, and it introduces two ethyl groups at the 5- and 6-positions via sequential regioselective Friedel-Crafts acetylations and hydrogenations of N-protected-2-aminoindan. The Friedel-Crafts acetylations can be carried out neat with high regioselectivity using acetyl chloride as the reagent as well as the solvent, thus avoiding the use of halogenated solvents.

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