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Ethanone, 2-(2-quinolinyl)-1-(2,4,6-trihydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101068-27-3

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101068-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101068-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101068-27:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*8)+(2*2)+(1*7)=73
73 % 10 = 3
So 101068-27-3 is a valid CAS Registry Number.

101068-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(2-quinolyl)-2,4,6-trihydroxyacetophenone

1.2 Other means of identification

Product number -
Other names 2-Quinolin-2-yl-1-(2,4,6-trihydroxy-phenyl)-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:101068-27-3 SDS

101068-27-3Downstream Products

101068-27-3Relevant articles and documents

ACETOFORMIC ANHYDRIDE IN THE SYNTHESIS OF CHROMONES. 1. SYNTHESIS OF 3-HETARYLCHROMONES

Pivovarenko, V. G.,Khilya, V. P.

, p. 496 - 501 (1991)

It was shown that the reaction of α-(het)aryl-2,4-dihydroxy- and 2,4,6-trihydroxyacetophenones with acetoformic anhydride catalyzed by sodium formate is an effective method for the preparation of chromones containing a heteroaromatic residue at the 3-position.The yield of the chromone and the rate of the reaction increase with increase in the ?-deficiency of this residue or in the presence of a hydroxy group in the 6-position of the starting acetophenone.In the last case the method is also applicable to the preparation of the difficulty available 3-aryl-5,7-dihydroxychromones.Chromones with a nitrogen-containing residue are formed without the use of any catalyst.

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