155831-46-2 Usage
Uses
Used in Pharmaceutical Industry:
2,4-dimethoxy-5-fluorobenzaldehyde is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure makes it a valuable building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dimethoxy-5-fluorobenzaldehyde serves as an intermediate in the production of agrochemicals. Its role in the synthesis of these compounds helps in the development of effective solutions for agricultural applications, such as pest control and crop protection.
Used in Organic Compounds Production:
2,4-dimethoxy-5-fluorobenzaldehyde is also utilized as a building block in the production of various organic compounds. Its versatile chemical properties allow it to be incorporated into a wide range of organic synthesis processes, leading to the creation of diverse chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 155831-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,3 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155831-46:
(8*1)+(7*5)+(6*5)+(5*8)+(4*3)+(3*1)+(2*4)+(1*6)=142
142 % 10 = 2
So 155831-46-2 is a valid CAS Registry Number.
155831-46-2Relevant academic research and scientific papers
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.
Some fluoro and nitro analogues of hallucinogenic amphetamines
Jara,Torres,Cassels,Rezende
, p. 417 - 426 (2007/10/02)
The preparation of the fluoro and nitro analogues (2)-(5) of the hallucinogens 2,4,5-trimethoxy- and 2-methoxy-4,5-methylenedioxy-amphetamine is described.
