52225-85-1 Usage
General Description
2-(3-chloro-propyl)-pyridine is a chemical compound that consists of a pyridine ring with a propyl group attached to the third carbon and a chlorine atom bonded to the second carbon. It is often used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. The presence of the chlorine atom and the pyridine ring make it a versatile building block for the creation of various complex molecules. It is also used as a reagent in organic synthesis and as a chemical intermediate in the production of fine chemicals. The compound has potential applications in the pharmaceutical industry due to its ability to modify the activity and selectivity of certain drugs. Additionally, it can be used in research and development for the creation of new drugs and other biological compounds. Overall, 2-(3-chloro-propyl)-pyridine has diverse applications in the fields of organic chemistry and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 52225-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,2 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52225-85:
(7*5)+(6*2)+(5*2)+(4*2)+(3*5)+(2*8)+(1*5)=101
101 % 10 = 1
So 52225-85-1 is a valid CAS Registry Number.
52225-85-1Relevant articles and documents
Photocyclization reactions of cyclohexa- and cyclopenta-fused pyridinium salts. Factors governing regioselectivity
Zhao, Zhiming,Duesler, Eileen,Wang, Canhui,Guo, Hua,Mariano, Patrick S.
, p. 8508 - 8512 (2007/10/03)
The results of studies described in this report show that irradiation of 1,2-cyclopenta-fused pyridinium perchlorate in aqueous base promotes a remarkably regioselective photocyclization reaction that results in exclusive formation of a single tricyclic a
Association phenomena. IV. Catalysis of the ionization of dihydroxyacetone phosphate by monofunctional, and trifunctional amines
Gettys,Gutsche
, p. 141 - 159 (2007/10/04)
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