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4H-1-Benzopyran-4-one, 7-[(6-bromohexyl)oxy]-5-hydroxy-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873302-28-4

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873302-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873302-28-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,3,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 873302-28:
(8*8)+(7*7)+(6*3)+(5*3)+(4*0)+(3*2)+(2*2)+(1*8)=164
164 % 10 = 4
So 873302-28-4 is a valid CAS Registry Number.

873302-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(6-bromohexoxy)-5-hydroxy-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 7-(6-bromohexyloxy)-5-hydroxy-2-phenyl-4H-chromen-4-one

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:873302-28-4 SDS

873302-28-4Downstream Products

873302-28-4Relevant academic research and scientific papers

Study on the synthesis, antioxidant properties, and self-assembly of carotenoid–flavonoid conjugates

Línzembold, Ildikó,Czett, Dalma,B?ddi, Katalin,Kurtán, Tibor,Király, Sándor Balázs,Gulyás-Fekete, Gergely,Takátsy, Anikó,Lóránd, Tamás,Deli, József,Agócs, Attila,Nagy, Veronika

, (2020/02/11)

Flavonoids and carotenoids possess beneficial physiological effects, such as high antioxidant capacity, anticarcinogenic, immunomodulatory, and anti-inflammatory properties, as well as protective effects against UV light. The covalent coupling of hydropho

Novel photosensitizing properties of porphyrin–chrysin derivatives with antitumor activity in vitro

He, Jun,Liu, Ding,Liu, Yunmei,Long, Huizhi,Yu, Wenmei,Zhang, Lang,Zhang, Qizhi

, p. 494 - 504 (2020/03/23)

Photodynamic therapy is a promising cancer treatment with the advantages of low toxicity, high efficiency, and noninvasiveness. In this study, 23 novel porphyrin–chrysin derivatives are synthesized using alkyl carbon chains as bridges. We use human gastri

Synthesis, structural study and biological activity of new derivatives of chrysin containing a 2-mercaptopyridyl or 5-(trifluoromethyl)-2-mercaptopyridyl fragments

Valdez-Calderón, Alejandro,González-Montiel, Simplicio,Martínez-Otero, Diego,Martínez-Torres, Ataulfo,Vásquez-Pérez, José Manuel,Molina-Vera, Carlos,Torres-Valencia, J. Martín,Alvarado-Rodríguez, José G.,Cruz-Borbolla, Julian

, p. 196 - 207 (2016/02/05)

New derivatives of chrysin containing 2-mercaptopyridine (2a-2e) or 5-(trifluoromethyl)-2-mercaptopyridine (3a-3e) moieties were prepared from the reaction between bromides (1a-1e) and 2-mercaptopyridine or 5-(trifluoromethyl)-2-mercaptopyridine, respecti

Synthesis, characterization and vasculoprotective effects of nitric oxide-donating derivatives of chrysin

Zou, Xiao-Qing,Peng, Sheng-Ming,Hu, Chang-Ping,Tan, Li-Feng,Yuan, Qiong,Deng, Han-Wu,Li, Yuan-Jian

experimental part, p. 3020 - 3025 (2010/07/05)

Vascular complications are major causes of disability and death in patients with diabetes mellitus. It is often characterized by endothelial dysfunction. Studies have shown that either the loss of nitric oxide bioactivity or the decreased biosynthesis of

FLAVANOID COMPOUNDS AND PROCESS FOR PREPARATION THEREOF

-

Page/Page column 22-23, (2010/09/17)

The present invention relates to flavanoid compounds of general formula (X1) wherein: R1 is selected from a group consisting of morpholinyl, N-methyl piperizinyl, piperidinyl and N,N'-dimethylamino groups, and n ranges from 3 to 6, a

Synthesis and promotion angiogenesis effect of chrysin derivatives coupled to NO donors

Peng, Sheng-Ming,Zou, Xiao-Qing,Ding, Hua-Lan,Ding, Yong-Lan,Lin, Yuan-Bin

scheme or table, p. 1264 - 1266 (2009/09/04)

Two types of new chrysin derivatives were prepared by coupling NO donors of alkyl nitrate and furazan derivatives and were fully characterized by 1H NMR and other techniques. These compounds were tested in human umbilical vein endothelial cells

Synthesis and biological evaluation of novel C (7) modified chrysin analogues as antibacterial agents

Suresh Babu,Hari Babu,Srinivas,Hara Kishore,Murthy,Rao, J. Madhusudana

, p. 221 - 224 (2007/10/03)

The natural product, chrysin (5,7-dihydroxy flavone), obtained from Oroxylum indicum, exhibits numerous biological activities including anticancer, anti-inflammatory, and antiallergic activities. Three series of chrysin analogues were prepared, in which c

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