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Ethanone, 1-(1H-indol-7-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104019-20-7

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104019-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104019-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104019-20:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*9)+(2*2)+(1*0)=67
67 % 10 = 7
So 104019-20-7 is a valid CAS Registry Number.

104019-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-Indol-7-yl)ethanone

1.2 Other means of identification

Product number -
Other names 7-acetyl indole

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:104019-20-7 SDS

104019-20-7Downstream Products

104019-20-7Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

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Paragraph 0135-0136, (2020/12/03)

Provided are a compounds comprising a first ligand LA of

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

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Page/Page column 60, (2011/04/14)

A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).

1,3-dicarboxamide-oxindoles as antiinflammatory agents

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, (2008/06/13)

1,3-Dicarboxamidooxindoles as antiinflammatory agents prepared by reaction of the 1-carbamoyloxindole with an isocyanate or by aminolysis of the corresponding alkyl 1-carbamoyloxindole-3-carboxylate.

THE SYNTHESIS OF 5- and 7-ACETYLINDOLE DERIVATIVES. I. THE PHOTOCHEMICAL REARRANGEMENT OF 1-ACETYLINDOLINE

Akagi, Masao,Ozaki, Kazuko

, p. 61 - 64 (2007/10/02)

5- and 7-Acetyl substituted indole derivatives have been prepared via intramolecular photo rearrangement of acyl radical and intramolecular electrophilic acylation of 1-acetylindoline.

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