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Methanone, (3,5-diphenyl-2-thienyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27895-87-0

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27895-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27895-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,9 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27895-87:
(7*2)+(6*7)+(5*8)+(4*9)+(3*5)+(2*8)+(1*7)=170
170 % 10 = 0
So 27895-87-0 is a valid CAS Registry Number.

27895-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-diphenylthiophen-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names (3,5-diphenyl-thiophen-2-yl)-phenyl-methanone

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:27895-87-0 SDS

27895-87-0Downstream Products

27895-87-0Relevant academic research and scientific papers

A novel reaction of 2,4,6-triphenyl(thio)selenopyrylium salts leading to benzoyl(thio)selenophenes and 2,4,6-triphenyl(thio)selenopyrans

Drevko,Bol'Shakova,Almaeva,Suchkov,Mandych,Shekhter

experimental part, p. 1526 - 1527 (2011/01/06)

Thio- and selenopyrylium salts undergo simultaneous oxidation, leading to the corresponding benzoylselenophene or benzoylthiophene, and reduction reactions leading to 4H-selenopyran or 4H-thiopyran In the presence of water and triethylamine .

Facile synthesis of 2-aroyl-3,5-diarylthiophene

Wang, Jin-Xian,Shi, Xiaoning,Men, Xiuqin,Zhao, Lianbiao

, p. 2849 - 2856 (2007/10/03)

2-Aroyl-3,5-diarylthiophenes were prepared in very good yields by reaction of 2,4,6-triarylpyrylium salts or 2,4,6-triarylthiopyrylium salts with an aqeous solution of sodium sulfide and iodine at room temperature.

Palladium-catalyzed multiple arylation of thiophenes

Okazawa, Toru,Satoh, Tetsuya,Miura, Masahiro,Nomura, Masakatsu

, p. 5286 - 5287 (2007/10/03)

Secondary 2-thiophenecarboxamides efficiently undergo unique triarylation accompanied by formal decarbamoylation under palladium catalysis. 3-Substituted thiophenes, especially having an electron-withdrawing group, can also be triarylated. Copyright

Oxidation reactions of 4H-chalcogenopyrans

Drevko,Smushkin,Kharchenko

, p. 777 - 780 (2007/10/03)

We have studied the oxidation of 4H-chalcogenopyrans and chalcogenopyrylium salts by lead tetraacetate. We have established that the major reaction products on oxidation of 2,6-diphenyl-4H-thiopyran and selenopyran are 2,6-diphenyl-4H-thio(seleno)pyran-4-

Oxidation of 4H-Pyran, 4H-Thiopyran, and 4H-Selenopyran with Lead Tetraacetate

Drevko, B. I.,Smushkin, M. I.,Kharchenko, V. G.

, p. 1298 - 1299 (2007/10/03)

Oxidation of 2,4,6-triphenyl-4H-pyran, 2,4,6-triphenyl-4H-thiopyran, and 2,4,6-triphenyl-4H-selenopyran with lead tetraacetate yields, respectively, 2-benzoyl-3,5-diphenylfuran, 2-benzoyl-3,5-diphenylthiophene, and 2-benzoyl-3,5-diphenylselenophene.

OXIDATION OF 2,4,6-TRIARYL-4H-THIO(SELENO)PYRANS WITH SELENIUM DIOXIDE

Drevko, B. I.,Fomenko, L. Al,Kharchenko, V. G.

, p. 632 - 634 (2007/10/02)

The oxidation of 2,4,6-triaryl-4H-thio(seleno)pyrans with selenium oxide in pyridine was studied.It is shown that the corresponding 2,4-diaryl-5-aroylthiophenes and -selenophenes are formed as a result of the oxidation.

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