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147265-76-7

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147265-76-7 Usage

General Description

Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)- (9CI) is a chemical compound that consists of an ethanone group attached to a 1-(2,3-dihydro-1H-indol-6-yl) moiety. Ethanone, 1-(2,3-dihydro-1H-indol-6-yl)- (9CI) is a derivative of the indole ring system, which is commonly found in various natural and synthetic organic compounds. It may have potential applications in the fields of medicinal chemistry and pharmaceutical research due to its structural features and potential biological activities. Further research and study are needed to fully understand the properties and potential uses of this chemical compound.

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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