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111510-96-4

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111510-96-4 Usage

General Description

2-Butyl-5-methylthiophene is a chemical compound that belongs to the family of thiophenes, which are heterocyclic compounds with a five-membered ring containing four carbon atoms and one sulfur atom. It is a fairly stable substance but can be reactive under certain conditions. This organic compound has a complex structure and its molecular formula is C9H14S. There is not a lot of information available regarding its specific properties or uses. However, thiophenes are commonly used in research and industries such as pharmaceuticals and materials science, so it's plausible that 2-butyl-5-methylthiophene may have similar applications.

Check Digit Verification of cas no

The CAS Registry Mumber 111510-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,1 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111510-96:
(8*1)+(7*1)+(6*1)+(5*5)+(4*1)+(3*0)+(2*9)+(1*6)=74
74 % 10 = 4
So 111510-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H14S/c1-3-4-5-9-7-6-8(2)10-9/h6-7H,3-5H2,1-2H3

111510-96-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B24943)  2-n-Butyl-5-methylthiophene, 97%   

  • 111510-96-4

  • 1g

  • 210.0CNY

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  • Alfa Aesar

  • (B24943)  2-n-Butyl-5-methylthiophene, 97%   

  • 111510-96-4

  • 5g

  • 776.0CNY

  • Detail
  • Alfa Aesar

  • (B24943)  2-n-Butyl-5-methylthiophene, 97%   

  • 111510-96-4

  • 25g

  • 2852.0CNY

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111510-96-4SDS

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 2-BUTYL-5-METHYLTHIOPHENE

1.2 Other means of identification

Product number -
Other names Thiophene,2-butyl-5-methyl

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:111510-96-4 SDS

111510-96-4Downstream Products

111510-96-4Relevant articles and documents

INVESTIGATION OF THE MECHANISM OF THE RECYCLIZATION OF FURANS TO THIOPHENES AND SELENOPHENES UNDER ACID-CATALYSIS CONDITIONS. 3. INVESTIGATION OF THE RECYCLIZATION OF HOMOLOGS AND FUNCTIONAL DERIVATIVES OF FURAN. QUANTUM-CHEMICAL CALCULATIONS OF THE OBJECTS OF THE RECYCLIZATION

Gubina, T. I.,Labunskaya, V. I.,Pankratov, A. N.,Trushin, S. A.,Kharchenko, V. G.

, p. 1393 - 1398 (1993)

The kinetics of the conversion of di-, tri-, and tetraalkylfurans to the corresponding thiophenes were investigated.A correlation between the reactivities and structures of the investigated furans was established.Quantum-chemical calculations of the objects of the recyclization were made.The calculated and experimental data on the reactivities of the investigated compounds were compared.The most likely pathway of the protonation of furans in their recyclization was determined on the basis of calculations of the total energies of the protonated forms.

MECHANISM OF RECYCLIZATION OF FURANS TO THIOPHENES AND SELENOPHENES UNDER ACID CATALYSIS. 1. KINETIC STUDIES OF THE REACTION OF 2,5-DIALKYLFURANS WITH HYDROGEN SULFIDE IN THE PRESENCE OF HYDROCHLORID ACID

Voronin, S. P.,Gubina, T. I.,Markushina, I. A.,Kharchenko, V. G.

, p. 1113 - 1117 (2007/10/02)

The transformation of 2,5-dialkylfurans to thiophene by reaction with hydrogen sulfide in the presence of hydrochloric acid was studied.The reaction was found to be first order with respect to the furan; the rate of consumption of the furan did not change with the increasing length of one of the alkyl substituents.Recrystalization in the presence of acid proceeds in two independent directions: through the formation of an intermediate dicarbonyl compound, and by direct conversion of the furan to a thiophene.Kinetic data showed that the reaction occurs mainly by the second route.

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