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4861-58-9

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4861-58-9 Usage

Chemical Properties

Clear, colorless liquid; blood, fried aroma.

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. Also used as flavoring agent for food.

Aroma threshold values

High strength odor, meaty type; recommend smelling in a 0.10% solution or less.

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

4861-58-9 Well-known Company Product Price

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  • Alfa Aesar

  • (B21885)  2-n-Pentylthiophene, 98%   

  • 4861-58-9

  • 5g

  • 280.0CNY

  • Detail
  • Alfa Aesar

  • (B21885)  2-n-Pentylthiophene, 98%   

  • 4861-58-9

  • 25g

  • 1037.0CNY

  • Detail

4861-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Pentylthiophene

1.2 Other means of identification

Product number -
Other names 2-pentylthiophene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:4861-58-9 SDS

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.

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