4861-58-9 Usage
Description
2-N-Pentylthiophene is an organic compound that belongs to the thiophene family. It is a clear, colorless liquid with a blood, fried aroma. 2-N-PENTYLTHIOPHENE is characterized by its high strength odor and meaty type, making it suitable for use in various applications due to its distinct properties.
Uses
Used in Organic Synthesis:
2-N-Pentylthiophene is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of new chemical bonds and the creation of a wide range of products.
Used in Pharmaceuticals:
In the pharmaceutical industry, 2-N-Pentylthiophene is utilized as a vital raw material for the development of new drugs. Its chemical properties make it a promising candidate for the synthesis of therapeutic agents.
Used in Agrochemicals:
2-N-Pentylthiophene is also employed in the agrochemical sector as a starting material for the production of various agrochemical products, such as pesticides and herbicides.
Used in Dyestuff:
2-N-PENTYLTHIOPHENE is used as an important intermediate in the synthesis of dyestuff, contributing to the development of new and vibrant colors for various applications.
Used as a Flavoring Agent in the Food Industry:
Due to its distinct blood, fried aroma, 2-N-Pentylthiophene is used as a flavoring agent in the food industry. Its high strength odor and meaty type make it an ideal choice for enhancing the taste and aroma of various food products. It is recommended to smell this compound in a 0.10% solution or less to fully appreciate its aroma.
Check Digit Verification of cas no
The CAS Registry Mumber 4861-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4861-58:
(6*4)+(5*8)+(4*6)+(3*1)+(2*5)+(1*8)=109
109 % 10 = 9
So 4861-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H14S/c1-2-3-4-6-9-7-5-8-10-9/h5,7-8H,2-4,6H2,1H3
4861-58-9Relevant articles and documents
Photocatalytic degradation of benzothiophene by a novel photocatalyst, removal of decomposition fragments by MCM-41 sorbent
Hosseini, Asma,Faghihian, Hossein
, p. 2383 - 2401 (2019/01/29)
In this study, a catalyst was synthesized by introduction of ZnO onto the surface of FSM-16 catalyst support (ZnO/FSM-16). Impregnation of catalyst support by ZnO proceeded through reacting of FSM-16 nanoparticles with Zn(CH3COO)2 solution followed by calcination of the product. The synthesized photocatalyst was then identified by different methods, and the optical property of the photocatalyst was studied by the DRS method. The results showed that after deposition of photocatalyst on FSM-16 support, the photocatalyst band gap was shifted to the visible region. The photoluminescence studies revealed lower recombination of electron–holes of the photocatalyst after immobilization on FSM-16. The influence of different variables on the photocatalytic performance of the samples was studied. Under optimized conditions, the high degradation efficiency of 97% was obtained by ZnO/FSM-16. The compounds produced from degradation of benzothiophene were recognized by the GC–MS method, and the products containing sulfur were properly adsorbed by MCM-41 sorbent. The photocatalyst showed high regeneration capability, and its activity was mostly preserved after six regeneration cycles.
Addition of carbon nucleophiles to aldehyde tosylhydrazones of aromatic and heteroaromatic-compounds: Total synthesis of piperine and its analogs
Chandrasekhar,Venkat Reddy,Srinivasa Reddy,Ramarao
, p. 2667 - 2670 (2007/10/03)
Addition of carbon nucleophiles to aldehyde tosylhydrazones of aromatic and heteroaromatic compounds is reported. New observations have been made wherein alkylative reduction is observed in some cases whereas alkylative fragmentation is noticed in others. These findings are exploited in the synthesis of the useful alkaloid piperine and its analogs. (C) 2000 Elsevier Science Ltd.
