73825-93-1 Usage
Description
3-((E)-[4-(dimethylamino)phenyl]methylideneamino)propan-1-ol, also known as 3-((E)-N-(4-dimethylaminobenzylidene)amino)propan-1-ol, is a phenylmethylamine derivative belonging to the class of organic compounds. It is a pale yellow solid with a molecular formula of C13H18N2O and a molecular weight of 218.29 g/mol. 3-((E)-[4-(dimethylamino)phenyl]methylideneamino)propan-1-ol features a propylamine backbone and a 4-dimethylaminobenzylidene substituent, making it a valuable building block in pharmaceutical research and a potential therapeutic agent for various medical conditions.
Uses
Used in Pharmaceutical Research:
3-((E)-[4-(dimethylamino)phenyl]methylideneamino)propan-1-ol is used as a building block for the synthesis of other compounds in pharmaceutical research. Its unique structure and functional groups make it a versatile component in the development of new drugs and therapeutic agents.
Used in Medical Treatments:
3-((E)-[4-(dimethylamino)phenyl]methylideneamino)propan-1-ol is used as a potential therapeutic agent for the treatment of several medical conditions. Its specific applications and target conditions may vary, but its potential as a treatment option is supported by its presence in pharmaceutical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 73825-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,2 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73825-93:
(7*7)+(6*3)+(5*8)+(4*2)+(3*5)+(2*9)+(1*3)=151
151 % 10 = 1
So 73825-93-1 is a valid CAS Registry Number.
73825-93-1Relevant articles and documents
Bite angle effect of bidentate P-N ligands in palladium catalysed allylic alkylationf
Van Haaren, Richard J.,Druijven, Cees J. M.,Van Strijdonck, Gino P. F.,Oevering, Henk,Reek, Joost N. H.,Kamer, Paul C. J.,Van Leeuwen, Piet W. N. M.
, p. 1549 - 1554 (2007/10/03)
Two series of new bidentate P-N ligands have been synthesized. Application of these ligands in the palladium catalysed allylic alkylation of crotyl chloride and cinnamyl chloride leads to the preferential formation of the branched product. A larger bite angle of the ligand leads to higher regioselectivity. Stoichiometric alkylation of the complex [Pd(C4H7){p-MeOC6H4C=N(CH 2)4OPPh2}][O3SCF3] proceeds with 88% regioselectivity to the branched product. The Royal Society of Chemistry 2000.
