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4H-1-Benzopyran-4-one, 7-hydroxy-5,6-dimethoxy-2-phenyl-, also known as Apigenin 7-O-glucoside or Acacetin 7-O-glucoside, is a naturally occurring flavonoid compound found in various plants, including chamomile and parsley. This chemical is characterized by its 4H-1-benzopyran-4-one structure, with a hydroxyl group at the 7th position, two methoxy groups at the 5th and 6th positions, and a phenyl group at the 2nd position. It is known for its antioxidant, anti-inflammatory, and anticancer properties, making it a subject of interest in pharmaceutical and nutraceutical research. The compound's potential health benefits are being studied for various applications, including the treatment of cardiovascular diseases and cancer prevention.

2035-05-4

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2035-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2035-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2035-05:
(6*2)+(5*0)+(4*3)+(3*5)+(2*0)+(1*5)=44
44 % 10 = 4
So 2035-05-4 is a valid CAS Registry Number.

2035-05-4SDS

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 7-hydroxy-5,6-dimethoxy-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-one,7-hydroxy-5,6-dimethoxy-2-phenyl

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:2035-05-4 SDS

2035-05-4Relevant academic research and scientific papers

O-methylation of flavonoids by cell-free extracts of calamondin orange

Brunet, Gunter,Ibrahim, Ragai K.

, p. 741 - 746 (1980)

Cell-free extracts of calamondin orange (Citrus mitis) catalysed the O-methylation of almost all hydroxyls of a number of flavonoids, indicating the existence in citrus tissues of ortho, meta, para and 3-O-methyltransferases. The latter, hitherto unreported enzyme, catalysed the formation of 3-O-methyl ethers of galangin and quercetin. The stepwise O-methylation of a number of compounds, especially quercetin and quercetagetin, tends to suggest a coordinated sequence of O-methylations on the surface of a multienzyme complex. The methyl acceptor abilities of the flavonoid substrates used are discussed in relation to their hydroxyl substitution patterns and their negative electron density distribution.

Gastroprotective flavone/flavanone compounds with therapeutic effect on inflammatory bowel disease

-

, (2008/06/13)

PCT No. PCT/KR97/00144 Sec. 371 Date Jan. 14, 1999 Sec. 102(e) Date Jan. 14, 1999 PCT Filed Jul. 25, 1997 PCT Pub. No. WO98/04541 PCT Pub. Date Feb. 5, 1998The present invention relates to novel flavone/flavanone compounds or their pharmaceutically acceptable salts and process for preparation thereof for protecting gastrointestinal tracts against gastritis, ulcers and inflammatory bowel disease.

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