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

61445-49-6

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61445-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61445-49-6 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61445-49:
(7*6)+(6*1)+(5*4)+(4*4)+(3*5)+(2*4)+(1*9)=116
116 % 10 = 6
So 61445-49-6 is a valid CAS Registry Number.

61445-49-6SDS

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 bis(3,4-dihydroxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone, bis(3,4-dihydroxyphenyl)-

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:61445-49-6 SDS

61445-49-6Relevant academic research and scientific papers

AIE (AIEE) and mechanofluorochromic performances of TPE-methoxylates: Effects of single molecular conformations

Qi, Qingkai,Liu, Yifei,Fang, Xiaofeng,Zhang, Yumo,Chen, Peng,Wang, Yi,Yang, Bing,Xu, Bin,Tian, Wenjing,Zhang, Sean Xiao-An

, p. 7996 - 8002 (2013/07/19)

Two methoxy-substituted tetraphenylethylene (TPE) derivatives, tetra(4-methoxyphenyl)ethylene (TMOE) and tetra(3,4-dimethoxyphenyl)ethylene (TDMOE), were synthesized by McMurry reaction in high yields. The nearly centrosymmetric and natural propeller shape of TMOE and TDMOE excluded intermolecular effects, such as H or J-aggregation and π-π stacking, on their AIE (AIEE) and mechanofluorochromic performance. The crystal structures of TMOE and TDMOE, and theoretical calculations proved that their emission colours are determined by single molecular conjugation. These molecules were used to investigate pure conformational effects on molecular emissions. The spectral properties of these molecules in five environments of crystal(s), THF solution, THF-water binary solution, solidified THF and amorphous states, were investigated. The crystalline to amorphous phase transition by grinding resulted in good mechanofluorochromic performances with high quantum yields and distinguishable emission change, which was further explored as anti-counterfeiting inks on banknotes.

Bromophenols as inhibitors of protein tyrosine phosphatase 1B with antidiabetic properties

Shi, Dayong,Li, Jing,Jiang, Bo,Guo, Shuju,Su, Hua,Wang, Tao

, p. 2827 - 2832 (2012/06/01)

A series of bromophenol derivatives were synthesized and evaluated as protein tyrosine phosphatase 1B (PTP1B) inhibitors in vitro and in vivo based on bromophenol 4e (IC50 = 2.42 μmol/L), which was isolated from red algae Rhodomela confervoides

Inhibition of human carbonic anhydrase isozymes I, II and VI with a series of bisphenol, methoxy and bromophenol compounds

Balaydin, Halis Tuerker,Durdagi, Serdar,Ekinci, Deniz,Sentuerk, Murat,Goeksu, Sueleyman,Menzek, Abdullah

, p. 467 - 475 (2012/09/08)

Carbonic anhydrase inhibitors (CAI) are valuable molecules as they have several therapeutic applications, including anti-glaucoma activity. In this study, inhibition of three human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and VI with a series o

Bromophenols as Candida albicans isocitrate lyase inhibitors

Oh, Ki-Bong,Jeon, Heung Bae,Han, Yu-Ri,Lee, Yeon-Ju,Park, Jiyoung,Lee, So-Hyoung,Yang, Dongsik,Kwon, Mihyun,Shin, Jongheon,Lee, Hyi-Seung

scheme or table, p. 6644 - 6648 (2010/12/19)

A new series of bromophenols was synthesized by reactions of corresponding phenol analogs with bromine. The synthesized compounds were tested for inhibitory activity against isocitrate lyase (ICL) of Candida albicans and antimicrobial activity against Gram-positive and, Gram-negative bacteria and fungi. Among the synthesized bromophenols, bis(3-bromo-4,5-dihydroxyphenyl) methanone (11) and (3-bromo-4,5-dihydroxyphenyl)(2,3-dibromo-4,5- dihydroxyphenyl)methanone (12) displayed potent inhibitory activities against ICL, showing a stronger inhibitory effects than were found with natural bromophenol 1. The preliminary structure-activity relationships were investigated in order to determine the essential structural requirements for the inhibitory activities of these compounds against ICL of C. albicans.

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