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Thiophene, 3-[4-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145208-63-5

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145208-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145208-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,0 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145208-63:
(8*1)+(7*4)+(6*5)+(5*2)+(4*0)+(3*8)+(2*6)+(1*3)=115
115 % 10 = 5
So 145208-63-5 is a valid CAS Registry Number.

145208-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-tert-butylphenyl)thiophene

1.2 Other means of identification

Product number -
Other names -

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:145208-63-5 SDS

145208-63-5Relevant academic research and scientific papers

Redox-Divergent Construction of (Dihydro)thiophenes with DMSO

Chen, Qing-An,He, Gu-Cheng,Hu, Yan-Cheng,Ji, Ding-Wei,Liu, Heng,Zhang, Xiang-Xin,Zhao, Chao-Yang

supporting information, p. 24284 - 24291 (2021/10/08)

Thiophene-based rings are one of the most widely used building blocks for the synthesis of sulfur-containing molecules. Inspired by the redox diversity of these features in nature, we demonstrate herein a redox-divergent construction of dihydrothiophenes, thiophenes, and bromothiophenes from the respective readily available allylic alcohols, dimethyl sulfoxide (DMSO), and HBr. The redox-divergent selectivity could be manipulated mainly by controlling the dosage of DMSO and HBr. Mechanistic studies suggest that DMSO simultaneously acts as an oxidant and a sulfur donor. The synthetic potentials of the products as platform molecules were also demonstrated by various derivatizations, including the preparation of bioactive and functional molecules.

A new polythiophene-driven coating method on an inorganic INT/IF-WS2 nanomaterial surface

Raichman,Ben-Shabat Binyamini,Lellouche

, p. 4490 - 4504 (2016/01/29)

Inorganic nanotubes and fullerene nanoparticles of tungsten disulfide (INTs-WS2 and IFs-WS2, respectively) are practically inert, hindering their usefulness in both research and commercial applications. The covalent attachment of fun

Suzuki-Miyaura coupling of aryl tosylates and mesylates in water

Pschierer, Jan,Plenio, Herbert

experimental part, p. 2934 - 2937 (2010/08/07)

The palladium complex (0.5 mol-%) of a water-soluble sulfonated fluorenylphosphane (cataCXium Fsulf) enables the facile Suzuki-Miyaura coupling of various (heterocyclic) aryl tosylates and aryl mesylate with various (heterocyclic) boronic acids in excellent yields (> 95%) using water as the reaction solvent.

A general palladium catalyst system for suzuki-miyaura coupling of potassium aryltrifluoroborates and aryl mesylates

Chow, Wing Kin,So, Chau Ming,Lau, Chak Po,Kwong, Fuk Yee

supporting information; scheme or table, p. 5109 - 5112 (2010/09/05)

(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of aryl and heteroaryl mesylates with potassium aryl and heteroaryltrifluoroborates are presented. In addition to biaryl couplings, the cross-coupling reactions of aryl mesylates with alkyl and vinyltrifluoroborate salts have also been successfully accomplished.

Novel Immunosuppressive Butenamides

Axton, Christopher A.,Billingham, Michael E. J.,Bishop, Paul M.,Gallagher, Peter T.,Hicks, Terence A.,et al.

, p. 2203 - 2214 (2007/10/02)

2-thiophene 12 was carboxylated using butyllithium and carbon dioxide to give 5-thiophene-2-carboxylic acid 13.Conversion of the acid 13 using diphenyl phosphazidate and triethylamine gave 5-4-(1,

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