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2-(2-methoxyphenyl)-4H-benzo[h]chromen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14756-21-9

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14756-21-9 Usage

Chemical family

Benzochromenone

Close relation

Cannabinoids found in cannabis, specifically cannabichromene (CBC)

Unique property

2-methoxyphenyl group on the benzochromenone structure

Potential medicinal uses

Anti-inflammatory, anti-cancer, and neuroprotective effects

Possible treatment

Mood disorders, novel anti-epileptic agent

Check Digit Verification of cas no

The CAS Registry Mumber 14756-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,5 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14756-21:
(7*1)+(6*4)+(5*7)+(4*5)+(3*6)+(2*2)+(1*1)=109
109 % 10 = 9
So 14756-21-9 is a valid CAS Registry Number.

14756-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyphenyl)-4H-benzo[h]chromen-4-one

1.2 Other means of identification

Product number -
Other names 2'-methoxy-7,8-benzoflavone

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:14756-21-9 SDS

14756-21-9Downstream Products

14756-21-9Relevant academic research and scientific papers

Fungal metabolism of naphthoflavones

Pop?oński, Jaros?aw,Sordon, Sandra,Tronina, Tomasz,Bartmańska, Agnieszka,Huszcza, Ewa

, p. 1 - 6 (2015/05/05)

Naphthoflavones (benzoflavones) are synthetic flavonoids commonly used in drug metabolism studies as selective activators or inhibitors of cytochrome P-450 enzymes. Nowadays they are also used as a component of food supplements for body builders. There is

Synthesis of methoxybenzoflavones and assignments of their NMR data

Hwang, Doseok,Jo, Geunhyeong,Hyun, Jiye,Lee, Sung Dae,Koh, Dongsoo,Lim, Yoongho

experimental part, p. 62 - 67 (2012/08/08)

A phytotoxic root exudate from Acroptilon repens was identified as 7,8-benzoflavone, an inhibitor of cytochrome P450 1A2 and activator of cytochrome P450 3A4. The synthetic 5,6-benzoflavone also is a potent phytotoxin. Six 7,8-benzoflavones and eight 5,6-benzoflavones were synthesized in this study. The NMR data for a few of these compounds have been previously reported; however, the NMR data for most of them have not been reported. For reference purposes, the complete NMR data for the 14 benzoflavones are described.

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