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58881-56-4

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58881-56-4 Usage

General 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.

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.

58881-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromophenyl)-2-[2-(4-bromophenyl)-2-oxoethyl]sulfanylethanone

1.2 Other means of identification

Product number -
Other names 1,1'-bis-(4-bromo-phenyl)-2,2'-sulfanediyl-bis-ethanone

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:58881-56-4 SDS

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

scheme or table, 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.

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