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2H-1-Benzopyran,3,4-dihydro-6-methoxy-2-phenyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73110-83-5

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73110-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73110-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73110-83:
(7*7)+(6*3)+(5*1)+(4*1)+(3*0)+(2*8)+(1*3)=95
95 % 10 = 5
So 73110-83-5 is a valid CAS Registry Number.

73110-83-5Downstream Products

73110-83-5Relevant academic research and scientific papers

Excited state interactions in phenol/olefin bichromophoric compounds: Direct detection of an intramolecular exciplex

Galindo,Jimenez,Miranda,Tormos

, p. 1747 - 1748 (2000)

The emission from an intramolecular exciplex detected in trans-4-methoxy-2-(3-phenyl-2-propenyl)phenol (1) is the first direct evidence for the excited state interchromophoric interaction in phenol-styrene systems.

Regioselective Domino Synthesis of 2-Alkylflavans via Hidden Br?nsted Acid Catalysis

Jin, Ha Jeong,Kim, Jae Hyung,Kang, Eun Joo

supporting information, p. 3137 - 3144 (2017/07/12)

A range of alkyl-substituted flavans, which are important structural elements in natural products and pharmaceutical molecules, were prepared by successive hidden Br?nsted acid catalyzed domino reaction, intermolecular hydroarylation, and intramolecular hydroalkoxylation. 1,1-Disubstituted allenes were activated under mild acidic AgOTf/t-BuCl condition to initiate the regioselective Friedel-Crafts reaction with phenol derivatives, and the consecutive reaction triggered by the 6 -endo cyclization led to the formation of a new type of 2-alkylflavan. Mechanistic study of the reaction intermediates and control experiments support the catalytic pathway and advantage of hidden Bronsted acid catalysis.

Pt(IV)-catalyzed generation and [4+2]-cycloaddition reactions of o-quinone methides

Radomkit, Suttipol,Sarnpitak, Pakornwit,Tummatorn, Jumreang,Batsomboon, Paratchata,Ruchirawat, Somsak,Ploypradith, Poonsakdi

, p. 3904 - 3914 (2011/06/22)

Novel intermolecular and intramolecular generations of ortho-quinone methides and their formal [4+2]-cycloaddition reactions with olefins catalyzed by PtCl4 and AuCl3 under mild conditions have been developed. Good to excellent yields (up to 99%) and diastereoselectivity (up to >99:1) of the chromans were obtained. PtCl4 was found to be effective and compatible with various functional groups present in the substrates. A mechanism accounting for its catalytic cycle is proposed and discussed.

Intramolecular excited-state interactions in phenol-styrene bicromophoric systems: A photochemical and photophysical study

Consuelo Jiménez,Miranda, Miguel A,Tormos, Rosa

, p. 115 - 120 (2007/10/03)

The intramolecular excited state interaction between phenol and styrene in a series of trans-2-cinnamylphenols bearing electron-donating substituents at the phenolic ring has been directly observed as an exciplex emission in acetonitrile. The photochemica

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