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50276-98-7

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50276-98-7 Usage

General Description

3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde is a chemical compound with the molecular formula C10H8O3. It is a derivative of benzopyran, a type of organic compound with a benzene ring fused to a pyran ring. The compound is also known as 5-formyl-2,3-dihydro-2-benzofuran-1(3H)-one and is commonly used in chemical and pharmaceutical research. It is a white to off-white solid with a melting point of around 118-120°C and a boiling point of 330.6°C. The compound may have potential applications in the development of pharmaceuticals and other industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 50276-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,7 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50276-98:
(7*5)+(6*0)+(5*2)+(4*7)+(3*6)+(2*9)+(1*8)=117
117 % 10 = 7
So 50276-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O3/c11-6-7-2-1-3-9-8(7)4-5-13-10(9)12/h1-3,6H,4-5H2

50276-98-7SDS

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 1-oxo-3,4-dihydroisochromene-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names Erythrocentaurin

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:50276-98-7 SDS

50276-98-7Relevant articles and documents

Structure elucidation of metabolites of swertiamarin produced by Aspergillus niger

Jun, Chang,Xue-Ming, Zhao,Chang-Xiao, Liu,Tie-Jun, Zhang

, p. 22 - 25 (2008)

The in vitro metabolism of swertiamarin was carried out in preparative scale using the fungus Aspergillus niger and the metabolites were isolated by semi-preparative HPLC combined with liquid-liquid extraction. Two metabolites, erythrocentaurin and one new compound were obtained and identified by 1H, 13C and 2D NMR and high resolution MS. The anti-inflammatory activity of the novel metabolite was tested and compared with that of swertiamarin in a mice model.

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