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126522-01-8

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  • 4H-Thieno[3,2-c][1]benzopyran-2-carboxylicacid, methyl ester

    Cas No: 126522-01-8

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126522-01-8 Usage

General Description

Methyl 4H-(1)-benzopyrano(4,3-b)thiophe is a chemical compound belonging to the class of benzopyran derivatives. It is a heterocyclic compound with a structure consisting of a benzopyran ring fused with a thiophene ring. METHYL 4H-(1)-BENZOPYRANO(4 3-B)THIOPHE& has potential applications in the field of medicinal chemistry and pharmaceuticals due to its diverse biological activities. It may act as an antioxidant, anti-inflammatory, or potential therapeutic agent for various diseases. Additionally, it may also find use in the field of organic synthesis and material science due to its unique structure and properties. However, further research is required to fully explore and understand its potential applications and biological functions.

Check Digit Verification of cas no

The CAS Registry Mumber 126522-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126522-01:
(8*1)+(7*2)+(6*6)+(5*5)+(4*2)+(3*2)+(2*0)+(1*1)=98
98 % 10 = 8
So 126522-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O3S/c1-15-13(14)11-6-8-7-16-10-5-3-2-4-9(10)12(8)17-11/h2-6H,7H2,1H3

126522-01-8 Well-known Company Product Price

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  • Aldrich

  • (560898)  Methyl4H-[1]-benzopyrano[4,3-b]thiophene-2-carboxylate  97%

  • 126522-01-8

  • 560898-1G

  • 484.38CNY

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126522-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4H-thieno[3,2-c]chromene-2-carboxylate

1.2 Other means of identification

Product number -
Other names UPCMLD-DP156

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:126522-01-8 SDS

126522-01-8Relevant articles and documents

Synthesis and Biological Activity of 4H-Thieno[3,2-c]Chromene Derivatives

Bogza, Yu. P.,Katsiel',Sharypova,Tolstikova,Fisyuk

, p. 1712 - 1718 (2015)

The formyl group of 4H-thieno[3,2-c]chromene-2-carbaldehyde was transformed into the respective nitrile, amide, ester, carboxylic, hydroxamic, or hydroxy group. Electrophilic substitution in 4H-thieno[3,2-c]chromene-2-carbaldehyde was shown to occur at the C-8 atom, while oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in methanol led to 4-methoxy-4H-thieno[3,2-c]chromene-2-carbaldehyde. The latter compound was found to possess high antiulcer activity.

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