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Methanone, (3,4-dihydroxyphenyl)(2,3,4-trihydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61445-51-0

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61445-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61445-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,4 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61445-51:
(7*6)+(6*1)+(5*4)+(4*4)+(3*5)+(2*5)+(1*1)=110
110 % 10 = 0
So 61445-51-0 is a valid CAS Registry Number.

61445-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4-dihydroxyphenyl)-(2,3,4-trihydroxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2,3,4,3',4'-Pentahydroxy-benzophenon

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:61445-51-0 SDS

61445-51-0Downstream Products

61445-51-0Relevant academic research and scientific papers

Synthesis and antioxidant properties of (3,4-dihydroxyphenyl)(2,3,4- trihydroxyphenyl)methanone and its derivatives

Cetinkaya, Yasin,Goecer, Huelya,Menzek, Abdullah,Guelcin, Ilhami

, p. 323 - 334 (2012/07/27)

(3,4-Dihydroxyphenyl)(2,3,4-trihydroxyphenyl)methanone (5) and its two derivatives with bromine were synthesized from reactions such as bromination and demethylation of (3,4-dimethoxyphenyl)(2,3,4-trimethoxyphenyl)methanone (6). The Wolf-Kishner reduction product (9) of 6 and its three derivatives with bromine were obtained. 4-(3,4-Dihydroxybenzyl)benzene-1,2,3-triol and its dibromide derivative (16) were also synthesized from 9 and the corresponding dibromide derivative. The in vitro antioxidant activities of nine new compounds synthesized in these reactions were determined by analyzing the radical scavenging activities of bromophenols for 2,2′-azino-bis(3- ethylbenzthiazoline-6-sulfonic acid) (ABTS), 1,1-diphenyl-2-picryl-hydrazyl (DPPH), N,N-dimethyl-p-phenylenediamine (DMPD), and the superoxide anion radical (O2-?) and examining the total reducing power through Fe3+-Fe2+ transformation, FRAP and CUPRAC assays and the ferrous ions (Fe2+) chelating activities. Moreover, the results of these activities were compared to those of standard antioxidant compounds such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), α-tocopherol, and trolox. The results showed that the synthesized bromophenols had effective antioxidant power. The phenol 5 with two phenolic rings and five phenolic hydroxyl groups was the most potent antioxidant and radical scavenger. In conclusion, the new compounds are promising molecules to be used owing to their potential antioxidant properties. (3,4-Dihydroxyphenyl) (2,3,4-trihydroxyphenyl)methanone (5) and its two derivatives with bromine were synthesized. 4-(3,4-Dihydroxybenzyl)benzene-1,2,3-triol and its dibromide derivative (16) were also synthesized. The in vitro antioxidant activities of nine new compounds were determined, showing that the synthesized bromophenols had effective antioxidant power. The phenol 5 with two phenolic rings and five phenolic hydroxyl groups was the most potent antioxidant and radical scavenger.

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