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4-phenylthiophene-3-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23062-42-2

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23062-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23062-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,6 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23062-42:
(7*2)+(6*3)+(5*0)+(4*6)+(3*2)+(2*4)+(1*2)=72
72 % 10 = 2
So 23062-42-2 is a valid CAS Registry Number.

23062-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylthiophene-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Phenylthiophen-4-carbonsaeure

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:23062-42-2 SDS

23062-42-2Relevant academic research and scientific papers

Catalyst-Controlled Regiodivergent Dehydrogenative Heck Reaction of 4-Arylthiophene/Furan-3-Carboxylates

Gao, Shang,Wu, Zijun,Wu, Fei,Lin, Aijun,Yao, Hequan

supporting information, p. 4129 - 4135 (2016/12/30)

A catalyst-controlled regiodivergent dehydrogenative Heck reaction of 4-arylthiophene/furan-3-carboxylates has been realized. Use of a palladium catalyst led to the C-5 alkenylation through electronic palladation, while a ruthenium catalyst favored the C-2 alkenylation with the assistance of a directing group. This reaction exhibited good to excellent regioselectivities. (Figure presented.).

Novel quinuclidinyl heteroarylcarbamate derivatives as muscarinic receptor antagonists

Nagashima, Shinya,Matsushima, Yuji,Hamaguchi, Hisao,Nagata, Hiroshi,Kontani, Toru,Moritomo, Ayako,Koshika, Tadatsura,Takeuchi, Makoto

, p. 3478 - 3487 (2014/06/23)

Herein, we describe the synthesis and pharmacological profiles of novel quinuclidinyl heteroarylcarbamate derivatives. Among them, the quinuclidin-4-yl thiazolylcarbamate derivative ASP9133 was identified as a promising long-acting muscarinic antagonist (LAMA) showing more selective inhibition of bronchoconstriction against salivation and more rapid onset of action in a rat model than tiotropium bromide.

Photochemical generation of thiophene analogs of 9-fluorenyl cations

Bancerz, Mathew,Huck, Lawrence A.,Leigh, William J.,Mladenova, Gabriela,Najafian, Katayoun,Zeng, Xiaofeng,Lee-Ruff, Edward

, p. 1202 - 1213 (2011/09/12)

The 9-fluorenyl cation is a member of the 4N Hueckel antiaromatic series of intermediates, first observed by time-resolved spectroscopy on UV photo-excitation of 9-fluorenol. Thiophene analogs of 9-fluorenol in which one of the annelated benzene rings is

COMPOUNDS THAT MODULATE INTRACELLULAR CALCIUM

-

Page/Page column 113, (2009/07/17)

Described herein are compounds and pharmaceutical compositions containing such compounds, which modulate the activity of store-operated calcium (SOC) channels. Also described herein are methods of using such SOC channel modulators, alone and in combinatio

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