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3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde, also known as 5-formyl-2,3-dihydro-2-benzofuran-1(3H)-one, is a chemical compound with the molecular formula C10H8O3. It is a derivative of benzopyran, characterized by a benzene ring fused to a pyran ring. This white to off-white solid has a melting point of approximately 118-120°C and a boiling point of 330.6°C. Its unique structure and properties make it a valuable compound in chemical and pharmaceutical research, with potential applications in the development of pharmaceuticals and other industrial products.

50276-98-7

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50276-98-7 Usage

Uses

Used in Pharmaceutical Research:
3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Chemical Research:
In the field of chemical research, 3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde serves as a valuable compound for studying the properties and reactions of benzopyran derivatives. Its reactivity and stability contribute to a better understanding of the chemical behavior of similar compounds.
Used in Industrial Product Development:
3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde may have potential applications in the development of various industrial products, such as dyes, pigments, and other specialty chemicals. Its unique properties can contribute to the creation of innovative and high-performance materials.
Used in Drug Synthesis:
3,4-Dihydro-1-oxo-1H-2-benzopyran-5-carbaldehyde is used as a building block in the synthesis of new drug candidates. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the development of novel therapeutic agents.

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 academic research and scientific papers

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.

Sweritranslactone D, a hepatoprotective novel secoiridoid dimer with tetracyclic lactone skeleton from heat-transformed swertiamarin

Zou, Ya-Dan,Ma, Xiao-Xia,Du, Sheng-Nan,Qi, Ping-Xing,He, Fang-Yan,Yang, Zhu-Ya,Tan, Wen-Hong,Khan, Afsar,Zhou, Zhi-Hong,Liu, Lu

, (2021)

Swertia mileensis, known as Qing-Ye-Dan (QYD), has been documented in Chinese Pharmacopoeia to cure hepatitis. Interestingly, its announced main active component, swertiamarin, could not be detected in the decoction, which indicated that the efficacy of QYD might be attributed to heat-transformed products of swertiamarin (HTPS). Further investigation on HTPS led to the isolation of sweritranslactone D (1), a novel secoiridoid dimer possessing a tetracyclic lactone skeleton, with better hepatoprotective activity than N-acetyl-L-cysteine in vitro.

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