58881-56-4 Usage
Description
1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE is a chemical compound with the molecular formula C16H13Br2O2S. It is a yellowish solid compound with a molecular weight of 407.14 g/mol. 1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE is commonly used in organic synthesis and pharmaceutical research as a building block for various chemical reactions. It contains two bromine atoms and a thioether group, making it suitable for applications in organic chemistry and drug discovery. Additionally, its aromatic structure and carbonyl functionality provide important reactivity for the synthesis of complex organic molecules and pharmacological intermediates.
Uses
Used in Organic Synthesis:
1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE is used as a building block for the synthesis of complex organic molecules. Its bromine atoms and thioether group contribute to its reactivity and versatility in organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE is used as a key intermediate in the development of new drugs. Its aromatic structure and carbonyl functionality make it a valuable component in the synthesis of pharmacological intermediates.
Used in Chemical Reactions:
1-(4-BROMO-PHENYL)-2-[2-(4-BROMO-PHENYL)-2-OXO-ETHYLSULFANYL]-ETHANONE is also utilized in various chemical reactions due to its unique structure and reactivity. The presence of bromine atoms and a thioether group allows for a wide range of reactions, making it a valuable asset in the field of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 58881-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,8 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58881-56:
(7*5)+(6*8)+(5*8)+(4*8)+(3*1)+(2*5)+(1*6)=174
174 % 10 = 4
So 58881-56-4 is a valid CAS Registry Number.
58881-56-4Relevant articles and documents
Synthesis of Phenanthro[9,10-c]thiophenes by 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)-Promoted Cyclo-Oxidation
Gao, Han,Connors, David M.,Goroff, Nancy S.
, p. 630 - 633 (2019/05/21)
A new method to prepare phenanthro[9,10-c]thiophenes has been developed. In the presence of triflic acid, 3,4-diaryl thiophenes undergo 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)-promoted cyclo-oxidation. NMR and computational studies indicate that p
Asymmetric synthesis of chiral dihydrothiopyrans via an organocatalytic enantioselective formal thio [3 + 3] cycloaddition reaction with binucleophilic bisketone thioethers
Wang, Shengzheng,Zhang, Yongqiang,Dong, Guoqiang,Wu, Shanchao,Zhu, Shiping,Miao, Zhenyuan,Yao, Jianzhong,Li, Hao,Li, Jian,Zhang, Wannian,Sheng, Chunquan,Wang, Wei
supporting information, p. 5570 - 5573 (2013/11/19)
An unprecedented organocatalytic highly enantioselective approach to a 3,4-dihydro-2H-thiopyran scaffold with two contiguous stereogenic centers has been implemented through a formal thio [3 + 3] cycloaddition process involving a Michael-aldol condensation cascade sequence. Notably, a new class of binucleophilic bisketone thioethers is designed for the process. Furthermore, the fine-tuning of their reactivity enables the cascade process to proceed with highly regioselectively.
Synthesis of oxathiane and morpholine from acyclic precursors: A modified Mitsunobu reaction
Paul, Nidhin,Kaladevi, Selvam,Beneto, Arockiam Jesin,Muthusubramanian, Shanmugam,Bhuvanesh, Nattamai
, p. 6892 - 6901 (2012/09/11)
Synthesis of a set of isomeric 2,4,6-triarylmorpholines and 2,6-diaryloxathianes from the corresponding 1,5-diols has been described. The method provides an efficient route to six-membered heterocycles from acyclic diols and is found to be better than Mitsunobu procedure in yield and waste management. In a related study, the ring contraction of pyranone to two isomeric cyclopentenone derivatives through Nazarov reaction has been noticed.