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2-(4-Methoxyphenylthio)pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1128077-19-9

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1128077-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1128077-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,8,0,7 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1128077-19:
(9*1)+(8*1)+(7*2)+(6*8)+(5*0)+(4*7)+(3*7)+(2*1)+(1*9)=139
139 % 10 = 9
So 1128077-19-9 is a valid CAS Registry Number.

1128077-19-9Downstream Products

1128077-19-9Relevant academic research and scientific papers

Two-Step Synthesis of Unsymmetrical Diaryl Sulfides by Electrophilic Thiolation of Non-functionalized (Hetero)arenes

B?hm, Marvin J.,Golz, Christopher,Rüter, Isabelle,Alcarazo, Manuel

, p. 15026 - 15035 (2018/09/25)

This article reports the efficient preparation of a series of unsymmetrically substituted thioethers through a two-step procedure consisting of an initial metal-free C?H sulfenylation of electron-rich (hetero)arenes with newly prepared succinylthioimidazolium salts. Subsequent reaction of the arylthioimidazolium intermediates with Grignard reagents afford the desired thioethers. The synthetic protocol described is modular, scalable, and high yielding, and provides access to sulfides that are not easy to obtain through the existing methodologies. Importantly, no prefunctionalization of the initial (hetero)arene is required.

Preparation of sulfenyl pyrroles

Gillis, H. Martin,Greene, Lana,Thompson, Alison

experimental part, p. 112 - 116 (2009/06/18)

Sulfenyl groups are attracting interest as masking/protecting groups for pyrroles. A facile one-step synthesis of sulfenyl pyrroles, involving the reaction of pyrroles with N-(aryl- and alkylthio)phthalimides in the presence of MgBr2, is reported and the methodology extends to include sulfinyl pyrroles. The one-step procedure gives good yields and is more efficient and practical than current multistep protocols to sulfenyl pyrroles that involve thiocyanato pyrrolic intermediates. A convenient procedure for the synthesis of N-(aryl- and alkylthio)phthalimides is also reported. Georg Thieme Verlag Stuttgart.

Antidiabetic pyrrolecarboxylic acids

-

, (2008/06/13)

Certain pyrrolecarboxylic and pyrroleacetic acid derivatives substituted on the pyrrole ring with thioether groups, acyl groups, phenyl, substituted phenyl, phenoxy, substituted phenoxy, benzyl or halo and optionally substituted on the pyrrole nitrogen with alkyl, and the pharmaceutically acceptable salts thereof, are useful in lowering the blood glucose levels of hyperglycemic animals.

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