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59303-13-8

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59303-13-8 Usage

General Description

2-Methyl-5-propionylthiophene is a chemical compound with the molecular formula C8H10OS. It is a thiophene derivative with a methyl and propionyl group attached to the 2 and 5 positions, respectively. 2-Methyl-5-propionylthiophene is commonly used as a flavoring and fragrance agent in the food and beverage industry, providing a sweet, fruity, and burnt odor and taste. It is also used in the production of perfumes and may have potential applications in pharmaceuticals and agrochemicals due to its unique aromatic properties. However, it is important to handle this chemical with care as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 59303-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,0 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59303-13:
(7*5)+(6*9)+(5*3)+(4*0)+(3*3)+(2*1)+(1*3)=118
118 % 10 = 8
So 59303-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10OS/c1-3-7(9)8-5-4-6(2)10-8/h4-5H,3H2,1-2H3

59303-13-8 Well-known Company Product Price

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  • Aldrich

  • (CBR00320)  1-(5-Methyl-2-thienyl)propan-1-one  AldrichCPR

  • 59303-13-8

  • CBR00320-1G

  • 2,255.76CNY

  • Detail

59303-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-methylthiophen-2-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names 5-methyl-2-thiophenyl ethyl ketone

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:59303-13-8 SDS

59303-13-8Relevant articles and documents

Structurally uniform 1-hexene, 1-octene, and 1-decene oligomers: Zirconocene/MAO-catalyzed preparation, characterization, and prospects of their use as low-viscosity low-temperature oil base stocks

Nifant'ev, Ilya E.,Vinogradov, Alexander A.,Vinogradov, Alexey A.,Sedov, Igor V.,Dorokhov, Viktor G.,Lyadov, Anton S.,Ivchenko, Pavel V.

, p. 40 - 50 (2017/09/25)

An original approach to α-olefin oligomerization as well as novel thermally stable zirconocene catalysts for use in such reactions has been elaborated. The method reported allows the achievement of fractions of lightweight α-olefin oligomers up to 90% yields without considerable formation of byproducts like internal alkenes, alkanes, and higher oligomers. Trimers, tetramers, and pentamers of 1-hexene, 1-octene, and 1-decene were isolated as individual compounds and were hydrogenated. Viscosity characteristics of the isolated saturated and unsaturated hydrocarbons have been studied at various temperatures. The isolated saturated oligomers of 1-octene and 1-decene outperform the traditional electrophilic oligomerization products in terms of viscosity indexes, pour points, and low-temperature viscosity.

Synthesis and characterization of AlCl3 impregnated molybdenum oxide as heterogeneous nano-catalyst for the Friedel-Crafts acylation reaction in ambient condition

Jadhav, Arvind H.,Chinnappan, Amutha,Hiremath, Vishwanath,Seo, Jeong Gil

, p. 8243 - 8250 (2015/11/27)

Aluminum trichloride (AlCl3) impregnated molybdenum oxide heterogeneous nano-catalyst was prepared by using simple impregnation method. The prepared heterogeneous catalyst was characterized by powder X-ray diffraction, FT-IR spectroscopy, solid-state NMR spectroscopy, SEM imaging, and EDX mapping. The catalytic activity of this protocol was evaluated as heterogeneous catalyst for the Friedel-Crafts acylation reaction at room temperature. The impregnated MoO4(AlCl2)2 catalyst showed tremendous catalytic activity in Friedel-Crafts acylation reaction under solvent-free and mild reaction condition. As a result, 84.0% yield of acyl product with 100% consumption of reactants in 18 h reaction time at room temperature was achieved. The effects of different solvents system with MoO4(AlCl2)2 catalyst in acylation reaction was also investigated. By using optimized reaction condition various acylated derivatives were prepared. In addition, the catalyst was separated by simple filtration process after the reaction and reused several times. Therefore, heterogeneous MoO4(AlCl2)2 catalyst was found environmentally benign catalyst, very convenient, high yielding, and clean method for the Friedel-Crafts acylation reaction under solvent-free and ambient reaction condition.

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