56824-70-5 Usage
Uses
Used in Organic Synthesis:
(5-bromo-2-thienyl)(4-methylphenyl)methanone is utilized as a fundamental building block in the field of organic synthesis. Its unique structure allows for the creation of a wide range of complex organic molecules, making it a valuable component in this industry.
Used in Pharmaceutical Research:
In the pharmaceutical sector, (5-bromo-2-thienyl)(4-methylphenyl)methanone is explored for its potential applications. Its distinctive chemical properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Agrochemicals:
(5-bromo-2-thienyl)(4-methylphenyl)methanone also finds use in the agrochemical industry, where it may contribute to the development of novel products such as pesticides or other agricultural chemicals.
Used as a Research Reagent:
(5-bromo-2-thienyl)(4-methylphenyl)methanone is employed as a reagent in the preparation of various organic compounds, facilitating research and development in the chemical and related industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56824-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56824-70:
(7*5)+(6*6)+(5*8)+(4*2)+(3*4)+(2*7)+(1*0)=145
145 % 10 = 5
So 56824-70-5 is a valid CAS Registry Number.
56824-70-5Relevant academic research and scientific papers
Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols
Xia, Anjie,Qi, Xueyu,Mao, Xin,Wu, Xiaoai,Yang, Xin,Zhang, Rong,Xiang, Zhiyu,Lian, Zhong,Chen, Yingchun,Yang, Shengyong
supporting information, (2019/05/07)
A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.
Ytterbium(III) trifluoromethanesulfonate catalysed Friedel-Crafts acylation of substituted thiophenes
Su, Weike,Jin, Can
, p. 694 - 695 (2007/10/03)
Ytterbium(III) trifluoromethanesulfonate [Yb(OTf)3] has been used to catalyse Friedel-Crafts acylation of substituted thiophenes in different solvents to produce several intermediates of pharmaceuticals and pesticides with good yields. The amount of catalysis was discussed and Yb(OTf)3 could be reused without loss of activity.
