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

108932-41-8

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108932-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108932-41-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108932-41:
(8*1)+(7*0)+(6*8)+(5*9)+(4*3)+(3*2)+(2*4)+(1*1)=128
128 % 10 = 8
So 108932-41-8 is a valid CAS Registry Number.

108932-41-8SDS

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 2-thiophen-3-ylphenol

1.2 Other means of identification

Product number -
Other names 2-(3-thienyl)phenol

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:108932-41-8 SDS

108932-41-8Relevant academic research and scientific papers

Cu-Catalyzed Dehydrogenative C-O Cyclization for the Synthesis of Furan-Fused Thienoacenes

Mitsudo, Koichi,Kobashi, Yoshiaki,Nakata, Kaito,Kurimoto, Yuji,Sato, Eisuke,Mandai, Hiroki,Suga, Seiji

supporting information, p. 4322 - 4326 (2021/06/21)

The first Cu-catalyzed dehydrogenative C-O cyclization for the synthesis of furan-fused thienoacenes is described. A variety of heteroacenes including a thieno[3,2-b]furan or a thieno[2,3-b]furan skeleton were synthesized by intramolecular C-H/O-H coupling. The use of a mixed solvent of N-methyl-2-pyrrolidone, ethylene glycol monomethyl ether, and toluene was essential for suppressing side reactions and efficiently promoting the reaction. Double C-O cyclization was also conducted to afford highly π-expanded furan-fused thienoacenes.

DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS

-

Page/Page column 43; 59, (2013/04/13)

The present invention provides novel 6-substituted [1,2,4]triazolo[4,3-b]pyridazines that are agonists of Rev-Erb. These compounds, and pharmaceutical compositions comprising the same, are suitable means for treating any disease wherein the activation of Rev-Erb has therapeutic effects, for instance in inflammatory and circadian rhythm-related disorders or cardiometabolic diseases.

MULTICYCLIC COMPOUNDS AND METHODS OF USE THEREOF

-

Page/Page column 97, (2011/06/25)

Provided herein are multicyclic compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various neurological disorders, including but not limited to, psychosis and schizophrenia.

α1-Adrenoceptor agonists: The identification of novel α1A subtype selective 2′-heteroaryl-2-(phenoxymethyl)imidazolines

Bishop, Michael J.,Barvian, Kevin A.,Berman, Judd,Bigham, Eric C.,Garrison, Deanna T.,Gobel, Michael J.,Hodson, Stephen J.,Irving, Paul E.,Liacos, James A.,Navas, Iii, Frank,Saussy Jr., David L.,Speake, Jason D.

, p. 471 - 475 (2007/10/03)

Novel 2′-heteroaryl-2-(phenoxymethyl)imidazolines have been identified as potent agonists of the cloned human α1-adrenoceptors in vitro. The nature of the 2′-heteroaryl group can have significant effects on the potency, efficacy, and subtype selectivity in this series. α1A Subtype selective agonists have been identified.

The Synthesis of Hydroxyphenylthiophenes

Baldwin, Larry J.,Pakray, Sudabeh,Castle, Raymond N.,Lee, Milton L.

, p. 1667 - 1669 (2007/10/02)

The synthesis of the five isomeric methoxyphenylthiophenes is described.The methoxy compounds were hydrolyzed to yield the hydroxyphenylthiophenes.

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