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N-[(4E)-4-(1,3-benzothiazol-2(3H)-ylidene)-3-oxocyclohexa-1,5-dien-1-yl]-1-benzofuran-2-carboxamide is a complex organic compound with a molecular formula of C23H13N3O4S. It is characterized by a benzofuran-2-carboxamide core, which is connected to a cyclohexa-1,5-dien-1-yl group through an amide bond. The cyclohexa-1,5-dien-1-yl group features a 4-(1,3-benzothiazol-2(3H)-ylidene)-3-oxo moiety, which adds to the molecule's complexity. N-[(4E)-4-(1,3-benzothiazol-2(3H)-ylidene)-3-oxocyclohexa-1,5-dien-1-yl]-1-benzofuran-2-carboxamide is likely to be found in the realm of pharmaceuticals or as an intermediate in the synthesis of various chemical products due to its intricate structure and potential reactivity.

6016-57-5

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6016-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6016-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6016-57:
(6*6)+(5*0)+(4*1)+(3*6)+(2*5)+(1*7)=75
75 % 10 = 5
So 6016-57-5 is a valid CAS Registry Number.

6016-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-(2-quinolyl)indole

1.2 Other means of identification

Product number -
Other names 2-Fenil-3-(2'-chinolil)-indolo

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:6016-57-5 SDS

6016-57-5Downstream Products

6016-57-5Relevant academic research and scientific papers

Preparation of indoles from o-alkynyltrifluoroacetanilides through the aminopalladation-reductive elimination process

Cacchi, Sandro,Fabrizi, Giancarlo,Parisi, Luca M.

, p. 1889 - 1894 (2007/10/03)

The functionalized pyrrole nucleus contained in the indole system has been assembled via the palladium-catalyzed reaction of o-alkynyltrifluoroacetanilides with organic halides/triflates or allyl carbonates. In the presence of carbon monoxide, a three-com

2-Substituted 3-aryl- and 3-heteroarylindoles by the palladium-catalyzed reaction of o-trifluoroacetanilides with aryl bromides and triflates

Cacchi, Sandro,Fabrizi, Giancarlo,Lamba, Doriano,Marinelli, Fabio,Parisi, Luca M.

, p. 728 - 734 (2007/10/03)

The palladium-catalyzed reaction of aryl and heteroaryl bromides and triflates with o-alkynyltrifluoroacetanilides affords 2-substituted 3-aryl- and heteroarylindoles usually in excellent yield. The procedure can be applied to the synthesis of 2-substituted indole-3-carboxaldehydes.

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