40089-91-6 Usage
Uses
Used in Flavor and Fragrance Industry:
4-Octylpyridine is utilized as a flavor and fragrance agent, contributing to the production of perfumes and other consumer products. Its distinct properties allow it to enhance the sensory experience of these products.
Used in Pharmaceutical Industry:
As an intermediate, 4-Octylpyridine plays a crucial role in the synthesis of various pharmaceuticals. Its chemical structure is a building block for developing new drugs with potential therapeutic applications.
Used in Pesticide Industry:
Similarly, in the pesticide industry, 4-Octylpyridine serves as an intermediate in the production of pesticides, aiding in the development of effective and targeted pest control solutions.
Used in Optoelectronic Devices:
4-Octylpyridine has been studied for its potential use in organic light-emitting diodes and other optoelectronic devices. Its unique electronic and optical properties make it a promising candidate for advancing technology in this field.
Safety Note:
It is important to handle 4-Octylpyridine with care due to its potential harmful effects if ingested, inhaled, or if it comes into contact with the skin. Proper safety measures should be taken during its use and storage to mitigate any risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 40089-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,8 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40089-91:
(7*4)+(6*0)+(5*0)+(4*8)+(3*9)+(2*9)+(1*1)=106
106 % 10 = 6
So 40089-91-6 is a valid CAS Registry Number.
40089-91-6Relevant articles and documents
Tetraphosphine/palladium catalysed Suzuki cross-coupling reactions of aryl halides with alkylboronic acids
Kondolff, Isabelle,Doucet, Henri,Santelli, Maurice
, p. 3813 - 3818 (2007/10/03)
Through the use of [PdCl(C3H5)]2/cis,cis, cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane as a catalyst, a range of aryl bromides and chlorides undergoes Suzuki cross-coupling with alkylboronic acids in good yields. Several alkyl substituents such as ethyl, n-butyl, n-octyl, isobutyl or 2,2-dimethylpropyl on the alkylboronic acids have been successfully used. The functional group tolerance on the aryl halide is remarkable; substituents such as fluoro, methyl, methoxy, acetyl, formyl, benzoyl, nitro or nitrile are tolerated. Furthermore, this catalyst can be used at low loading, even for reactions of sterically hindered aryl bromides.
