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5069-26-1

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5069-26-1 Usage

Uses

2-Methyl-5-phenylthiophen is employed as intermediate for pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 5069-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5069-26:
(6*5)+(5*0)+(4*6)+(3*9)+(2*2)+(1*6)=91
91 % 10 = 1
So 5069-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10S/c1-9-7-8-11(12-9)10-5-3-2-4-6-10/h2-8H,1H3

5069-26-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L20420)  2-Methyl-5-phenylthiophene, 96%   

  • 5069-26-1

  • 1g

  • 537.0CNY

  • Detail
  • Alfa Aesar

  • (L20420)  2-Methyl-5-phenylthiophene, 96%   

  • 5069-26-1

  • 5g

  • 1914.0CNY

  • Detail

5069-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYL-5-PHENYLTHIOPHENE

1.2 Other means of identification

Product number -
Other names 5-phenyl-2-methylthiophene

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:5069-26-1 SDS

5069-26-1Relevant articles and documents

Programmed Synthesis of Tetra-Aryl Thiophenes with Stepwise, Ester-Controlled Regioselectivity

Messina, Cynthia,Ottenwaelder, Xavier,Forgione, Pat

supporting information, p. 7348 - 7352 (2021/10/01)

Herein, we report a modular synthetic route to access tetra-arylated thiophene compounds with four different substituents with programmed chemical control provided by an ester activating/directing group. This method enables the functionalization of indivi

Metalated Porous Phenanthroline-Based Polymers as Efficient Heterogeneous Catalysts for Regioselective C?H Activation of Heteroarenes

Tang, Yongquan,Dai, Zhifeng,Wang, Sai,Chen, Fang,Meng, Xiangju,Xiao, Feng-Shou

, p. 2469 - 2474 (2021/08/06)

Direct C?H bond activation of heterocycles as a step-economical and environmentally friendly approach to build the heterobiaryls motifs is highly attractive, but it still has a challenge to design and prepare a cheap and regioselective heterogeneous catal

Light-Controllable Ionic Conductivity in a Polymeric Ionic Liquid

Dolinski, Neil D.,Hawker, Craig J.,Hu, Jerry,Nie, Hui,Read de Alaniz, Javier,Schauser, Nicole S.,Segalman, Rachel A.

supporting information, p. 5123 - 5128 (2020/02/11)

Polymeric ionic liquids (PILs) have attracted considerable attention as electrolytes with high stability and mechanical durability. Light-responsive materials are enabling for a variety of future technologies owing to their remote and noninvasive manipula

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