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1-Oxo-1H-2-benzopyran-3-carbaldehyde, also known as 2-benzopyran-3-carboxaldehyde or 2H-chromen-3-carboxaldehyde, is an organic compound with the chemical formula C10H6O3. It is a derivative of the benzopyran ring system, which is a heterocyclic aromatic compound consisting of a benzene ring fused to a pyran ring. This aldehyde is characterized by the presence of a carbonyl group (C=O) at the 1-position and a formyl group (CHO) at the 3-position. It is a pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fragrances. Due to its reactivity, it can undergo various chemical reactions, such as condensation, oxidation, and reduction, making it a valuable building block in organic synthesis.

34328-51-3

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34328-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34328-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,2 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34328-51:
(7*3)+(6*4)+(5*3)+(4*2)+(3*8)+(2*5)+(1*1)=103
103 % 10 = 3
So 34328-51-3 is a valid CAS Registry Number.

34328-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name artimidinal

1.2 Other means of identification

Product number -
Other names 3-formyl-1H-2-benzopyran-1-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:34328-51-3 SDS

34328-51-3Downstream Products

34328-51-3Relevant academic research and scientific papers

Silver triflate/: P -TSA co-catalysed synthesis of 3-substituted isocoumarins from 2-alkynylbenzoates

Gianni, Jonathan,Pirovano, Valentina,Abbiati, Giorgio

, p. 3213 - 3219 (2018/05/17)

In this paper, we describe the silver triflate/p-toluenesulfonic acid co-catalysed synthesis of seventeen isocoumarins and two thieno[2,3-c]pyran-7-ones starting from 2-alkynylbenzoates and 3-alkynylthiophene-2-carboxylates, respectively. The reaction proceeds with absolute regioselectivity under mild reaction conditions and low catalyst loading, to afford the desired products in good to excellent yields. A conceivable reaction mechanism is proposed and supported by isotope-exchange tests, 1H NMR studies and ad hoc experiments.

Synthesis and characterization of 3-formyl-1H-2-benzopyran-1-one

Hussain, Mazhar,Ahmad, Hafiz Badaruddin,Shad, Muhammad Aslam,Hussain, Adeel,Shafiq, Zahid,Yousaf, Muhammad,Uzair, Muhammad

, p. 5473 - 5475,3 (2020/09/15)

Synthesis and characterization of 3-formyl-1H-2-benzopyran-1-one is reported through convenient three step method. Homophthalic acid and ethyloxalyl chloride were refluxed to afford isocoumarin 3-ethylcarboxylate, which was subsequently heated to reflux with ethanolic hydrazine hydrate to yield isocoumarin-3-hydrazide. The product is treated with ammoniacal solution of metaperiodate to synthesize 3-formyl-1H-2-benzopyran-1-one. All products were characterized by IR, NMR and mass spectral analysis. Physical and spectral data were in close agreement with those, reported in literature.

New Syntheses of trans-Artemidin, Artemidinal and Tetrahydrocapillarin

Chatterjea, J. N.,Mukherjee, Sanat K.,Bhakta, C.

, p. 359 - 361 (2007/10/02)

Convenient syntheses of the natural isocoumarins described in the title are reported starting from 3-bromomethylisocoumarin (2).Artemidinal (3) has been prepared in one step by subjecting 2 to Sommlet reaction. 3 on Perkin reaction using butyric anhydrid

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