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1785-95-1

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1785-95-1 Usage

Chemical Properties

light yellow powder

Check Digit Verification of cas no

The CAS Registry Mumber 1785-95-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1785-95:
(6*1)+(5*7)+(4*8)+(3*5)+(2*9)+(1*5)=111
111 % 10 = 1
So 1785-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H10O3/c17-14(10-6-2-1-3-7-10)13-15(18)11-8-4-5-9-12(11)16(13)19/h1-9,17H

1785-95-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A15333)  2-Benzoyl-1,3-indanedione, 98%   

  • 1785-95-1

  • 5g

  • 759.0CNY

  • Detail
  • Alfa Aesar

  • (A15333)  2-Benzoyl-1,3-indanedione, 98%   

  • 1785-95-1

  • 25g

  • 1972.0CNY

  • Detail

1785-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzoylindene-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-benzoyl-2H-indene-1,3-dione

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:1785-95-1 SDS

1785-95-1Relevant articles and documents

Palladium-Catalyzed Carbonylative Annulation Reactions Using Aryl Formate as a CO Source: Synthesis of 2-Substituted Indene-1,3(2H)-dione Derivatives

Zhang, Ying,Chen, Jing-Lei,Chen, Zhen-Bang,Zhu, Yong-Ming,Ji, Shun-Jun

, p. 10643 - 10650 (2015/11/18)

An efficient synthesis of 2-substituted indene-1,3(2H)-diones from stable and readily available 1-(2-halophenyl)-1,3-diones by employing phenyl formate as a CO source has been developed. The reaction occurred via palladium-catalyzed intramolecular carbonylative annulation using K3PO4 as a base and DMSO as a solvent at 95 °C. In this protocol, the reaction showed a broad substrate scope with good to excellent yields.

α,β-UNSATURATED THIO COMPOUNDS. SYNTHESIS OF MONOTHIOCARBONYL ANALOGS OF 2-BENZOYL-1,3-INDANEDIONE

Korchevin, N. A.,Usova, T. L.,Vasil'ev, A. V.,Dorofeev, I. A.,Usov, V. A.,Voronkov, M. G.

, p. 518 - 521 (2007/10/02)

Structural isomers of the monothiocarbonyl analogs of 2-benzoyl-1,3-indanedione were obtained. 1-Oxo-2-(α-hydroxybenzylidene)-3-indanethione was synthesized by the action of hydrogen sulfide on 2-benzoyl-1,3-indanedione in the presence of hydrogen chlorid

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