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109592-60-1

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109592-60-1 Usage

General Description

Picembrin 7-acetate is a natural chemical compound found in plants of the family Scrophulariaceae. It belongs to the class of flavonoids and is known for its antioxidant and anti-inflammatory properties. Studies have shown that picembrin 7-acetate exhibits potential neuroprotective effects, making it a promising candidate for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its ability to modulate intracellular signaling pathways and reduce oxidative stress has also led to research into its potential therapeutic applications in cancer and cardiovascular diseases. Overall, picembrin 7-acetate has emerged as a valuable natural compound with diverse pharmacological properties and potential for further development in the field of medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 109592-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109592-60:
(8*1)+(7*0)+(6*9)+(5*5)+(4*9)+(3*2)+(2*6)+(1*0)=141
141 % 10 = 1
So 109592-60-1 is a valid CAS Registry Number.

109592-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-5-Hydroxy-4-oxo-2-phenyl-3,4-dihydro-2H-chromen-7-yl acetate

1.2 Other means of identification

Product number -
Other names Formononetinacetat

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:109592-60-1 SDS

109592-60-1Relevant articles and documents

Reduction of flavanones by NaBH3CN in trifluoroacetic acid.

Lewin, G.,Bert, M.,Dauguet, J. C.,Dolley, J.,Menez, P. Le,et al.

, p. 939 - 944 (2007/10/02)

For our studies on the reduction of flavanones, we worked on flavanone itself and on some other derivatives, oxygenated on the B ring.Besides expected flavans and chalcanes, condensed compounds (dimers and trimers) are also obtained.Reaction begins with the reduction of carbonyl to methylene; all the other isolated products arise from the two possible and competitive reactions on the potential carbocation C-2 of the flavan system: a) reductive cleavage of heterocycle; b) electrophilic aromatic substitution.Reactivity of flavanones is correlated with substituents of B ring through their ?+ values. Key words: flavanones / sodium cyanoborhydride / trifluoroacetic acid / flavans / chalcanes / dimers

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