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147265-76-7

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147265-76-7 Usage

Description

Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)(9CI) is a chemical compound characterized by an ethanone group connected to a 1-(2,3-dihydro-1H-indol-6-yl) moiety. It is a derivative of the indole ring system, which is prevalent in a variety of natural and synthetic organic compounds. Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)(9CI) may hold promise in medicinal chemistry and pharmaceutical research due to its unique structural attributes and potential biological activities, although further investigation is required to fully elucidate its properties and applications.

Uses

Used in Pharmaceutical Research:
Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)(9CI) is utilized as a research compound for exploring its potential biological activities and medicinal properties. Its indole ring system, a common structural motif in many bioactive molecules, suggests that it may interact with biological targets and pathways relevant to drug discovery.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)(9CI) serves as a starting material or a building block for the synthesis of more complex molecules with therapeutic potential. Its structural features may be optimized to enhance its pharmacological properties, such as potency, selectivity, and bioavailability.
Note: Since the provided materials do not specify particular applications or industries for Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)(9CI), the uses listed above are general and based on the compound's potential in pharmaceutical research and medicinal chemistry. Further research would be necessary to identify specific applications and industries where this compound could be utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 147265-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,6 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 147265-76:
(8*1)+(7*4)+(6*7)+(5*2)+(4*6)+(3*5)+(2*7)+(1*6)=147
147 % 10 = 7
So 147265-76-7 is a valid CAS Registry Number.

147265-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Acetyl-2,3-dihydro-1H-indole

1.2 Other means of identification

Product number -
Other names 1-(2,3-DIHYDRO-1H-INDOL-6-YL)ETHANONE

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:147265-76-7 SDS

147265-76-7Downstream Products

147265-76-7Relevant articles and documents

Regioselective Friedel-Crafts Acylation of 1,2,3,4-Tetrahydroquinoline and Related Nitrogen Heterocycles: Effects of NH Protective Groups and Ring Size

Ishihara, Yuji,Tanaka, Toshimasa,Goto, Giichi

, p. 3401 - 3406 (2007/10/02)

Regioselectivity of the Friedel-Crafts acylation of the following nitrogen heterocyles was studied: 2,3-dihydro-1H-indoles 3, 1,2,3,4-tetrahydroquinolines 4, 2,3,4,5-tetrahydro-1H-1-benzazepines 5 and 1,2,3,4,5,6-hexahydro-1-benzazocines 6.It was found that though the ratio of regioisomers depends on ring size, it can be controlled by changing the NH protective groups.A molecular orbital (MO) calculation of the Lewis acid co-ordinated substrates gave a rational explanation of the regioselectivity.

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