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2,3-DIHYDROXY-4-METHOXYACETOPHENONE, also known as 1-(2,3-Dihydroxy-4-methoxyphenyl)ethanone, is a neuroprotective compound derived from Cynenchum paniculatum. It possesses antioxidant properties and is known for its neuroprotective and cognitive-enhancing activities.
Used in Pharmaceutical Industry:
2,3-DIHYDROXY-4-METHOXYACETOPHENONE is used as a neuroprotective agent for its potential role in the treatment of Alzheimer's disease. Its antioxidant activity helps protect neurons from oxidative stress and may contribute to cognitive enhancement.

708-53-2

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708-53-2 Usage

Preparation

Preparation by reaction of acetic acid on pyrogallol 1-methyl ether, ? with zinc chloride at reflux (155–160°) (Nencki reaction); ? with boron trifluoride on a steam bath (77%).

Check Digit Verification of cas no

The CAS Registry Mumber 708-53-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 708-53:
(5*7)+(4*0)+(3*8)+(2*5)+(1*3)=72
72 % 10 = 2
So 708-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-5(10)6-3-4-7(13-2)9(12)8(6)11/h3-4,11-12H,1-2H3

708-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3-dihydroxy-4-methoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2,3-Dihydroxy-4-methoxy-acetophenon

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:708-53-2 SDS

708-53-2Relevant academic research and scientific papers

Total synthesis of bulbophylol-B

Lin, Jinshun,Zhang, Weige,Jiang, Nan,Niu, Zeyu,Bao, Kai,Zhang, Liang,Liu, Dailin,Pan, Chao,Yao, Xinsheng

experimental part, p. 1938 - 1941 (2009/09/25)

The first total synthesis of bulbophylol-B (1) has been achieved with the longest linear sequence of 12 steps and an overall yield of 17.9% via a new and practical approach to construct the dihydrodibenz[b,f]oxepin skeleton employing Wittig, selective reduction, and intramolecular Ullmann reactions as key steps.

SELECTIVE DEMETHYLATIONS IN 2,3,4-TRIMETHOXYARYL CARBONYL COMPOUNDS

Kaisalo, Leena,Latvala, Anita,Hase, Tapio

, p. 645 - 648 (2007/10/02)

2,3,4-Trimethoxybenzaldehyde, -acetophenone and -benzoic acid give the corresponding 2,3-dihydroxy-4-methoxy compounds in good yield on treatment with BCl3.

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