58069-37-7 Usage
General Description
3-Octylpyridine is a chemical compound with the molecular formula C14H21N. It is an organic compound that belongs to the class of pyridines, which are aromatic heterocyclic compounds containing a ring of five carbon atoms and one nitrogen atom. 3-Octylpyridine is a colorless to pale yellow liquid with a strong and unpleasant odor. It is primarily used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a flavoring agent in the food industry. Additionally, 3-Octylpyridine has been studied for its potential use in anticancer drugs due to its ability to inhibit the growth of cancer cells. However, it is important to handle this chemical with caution as it may cause irritation to the eyes, skin, and respiratory system if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 58069-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,6 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58069-37:
(7*5)+(6*8)+(5*0)+(4*6)+(3*9)+(2*3)+(1*7)=147
147 % 10 = 7
So 58069-37-7 is a valid CAS Registry Number.
58069-37-7Relevant 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.
