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3,4-Dihydro-2,4-diphenyl-2H-1-benzopyran, also known as diphenylbenzopyran, is a chemical compound with a benzopyran core structure. It is recognized for its potential anti-inflammatory and antioxidant properties, making it a promising candidate for pharmaceutical applications.
Used in Pharmaceutical Industry:
3,4-Dihydro-2,4-diphenyl-2H-1-benzopyran is used as a pharmaceutical compound for its potential to reduce inflammation and free radical damage. Its anti-inflammatory and antioxidant effects make it a candidate for the development of new drugs to treat various medical conditions.
Used in Drug Discovery and Development:
3,4-Dihydro-2,4-diphenyl-2H-1-benzopyran is used as a research compound in drug discovery and development due to its structure and physical properties. Further studies are required to fully understand its therapeutic benefits and biological activities, which could lead to the creation of novel treatments.

55256-25-2

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55256-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55256-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55256-25:
(7*5)+(6*5)+(5*2)+(4*5)+(3*6)+(2*2)+(1*5)=122
122 % 10 = 2
So 55256-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H18O/c1-3-9-16(10-4-1)19-15-21(17-11-5-2-6-12-17)22-20-14-8-7-13-18(19)20/h1-14,19,21H,15H2

55256-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diphenyl-3,4-dihydro-2H-chromene

1.2 Other means of identification

Product number -
Other names cis-2,4-diphenylchroman

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:55256-25-2 SDS

55256-25-2Downstream Products

55256-25-2Relevant academic research and scientific papers

Catalytic asymmetric synthesis of chiral phenols in ethanol with recyclable rhodium catalyst

Yao, Jian,Liu, Na,Yin, Long,Xing, Junhao,Lu, Tao,Dou, Xiaowei

supporting information, p. 4946 - 4950 (2019/09/30)

A general method to access diverse chiral phenols by rhodium-catalyzed asymmetric conjugate arylation using hydroxylated arylboronic acids in ethanol was developed. Recycling of the rhodium catalyst by flash chromatography on silica gel was feasible in this system. The synthetic utility of the strategy was demonstrated by efficient synthesis of chiral drug tolterodine.

Multicomponent Condensation Reactions via ortho-Quinone Methides

Allen, Emily E.,Zhu, Calvin,Panek, James S.,Schaus, Scott E.

, p. 1878 - 1881 (2017/04/11)

Iron(III) salts promote the condensation of aldehydes or acetals with electron-rich phenols to generate ortho-quinone methides that undergo Diels - Alder condensations with alkenes. The reaction sequence occurs in a single vessel to afford benzopyrans in up to 95% yield. The reaction was discovered while investigating a two-component strategy using 2-(hydroxy(phenyl)methyl)phenols to access the desired ortho-quinone methide in a Diels - Alder condensation. The two-component condensation also afforded the corresponding benzopyran products in yields up to 97%. Taken together, the two- and three-component strategies using ortho-quinone methide intermediates provide efficient access to benzopyrans in good yields and selectivities.

Heteroatom-Guided, Palladium-Catalyzed, Site-Selective C-H Arylation of 4H-Chromenes: Diastereoselective Assembly of the Core Structure of Myristinin B through Dual C-H Functionalization

Pawar, Govind Goroba,Tiwari, Virendra Kumar,Jena, Himanshu Sekhar,Kapur, Manmohan

supporting information, p. 9905 - 9911 (2015/06/30)

A highly site-selective, heteroatom-guided, palladium-catalyzed direct arylation of 4H-chromenes is reported. The C-H functionalization is driven not only by the substituents and structure of the substrate but also by the coupling partner being used. The diastereoselective assembly of the core structure of Myristinin B has been achieved by using a dual C-H functionalization strategy for regioselective direct arylation.

Gold-catalyzed oxa-povarov reactions for the synthesis of highly substituted dihydrobenzopyrans from diaryloxymethylarenes and olefins

Pagar, Vinayak Vishnu,Tseng, Chang-Chin,Liu, Rai-Shung

, p. 10519 - 10526 (2014/08/18)

Oxa-Povarov reactions involving readily available diaryloxymethylarenes and aryl-substituted alkenes are reported. Their [4+2] cycloadditions were efficiently catalyzed by IPrAuSbF6 (IPr=1,3-bis(diisopropylphenyl) imidazol-2-ylidene) with high diastereoselectivity. Product analysis revealed that the reactions likely proceed by a stepwise ionic mechanism, because both E- and Z-configured β-methylstyrene gave the same cycloadducts in the same proportions.

Hetero Diels-Alder reaction of olefin with o-quinone methides generated using (±)-binolphosphoric acid for the stereoselective synthesis of 2,4-diarylbenzopyrans: Application to the formal synthesis of myristinin B/C

Gharpure, Santosh J.,Sathiyanarayanan,Vuram, Prasanna K.

, p. 18279 - 18282 (2013/10/21)

Hetero Diels-Alder reaction of olefin with o-quinone methides (o-QMs) generated using (±)-binolphosphoric acid was developed for the stereoselective synthesis of 2,4-diarylbenzopyrans. The method thus developed was utilized in the formal synthesis of myri

Novel Generation of o-Quinone Methides on the Basis of Lewis Acid Catalyzed 1,4-Dethiolation of o-(1-(Alkylthio)alkyl)phenols

Inoue, Tsutomu,Inoue, Seiichi,Sato, Kikumasa

, p. 55 - 58 (2007/10/02)

The treatment of o-(1-(alkylthio)alkyl)phenols with Lewis acid resulted in the formation of o-quinone methides by the novel 1,4-dethiolation process, which, being activated with Lewis acid, reacted in situ with various dienophiles in the manner of Diels-Alder reaction in high efficiency. o-Quinone allide, provided from o-(1-(alkylthio)allyl)phenol, also behaved as heterodienes.

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