225236-02-2 Usage
General Description
Furan-2-ylmethyl-(2-methoxy-benzyl)-amine is a chemical compound with the molecular formula C13H15NO. It is a derivative of furan, a heterocyclic organic compound, and contains a benzyl group and an amine group. The presence of the furan ring and amine group makes it a versatile compound that can be used in various chemical reactions and organic synthesis processes. It may have potential applications in pharmaceuticals, agrochemicals, and other industries due to its unique chemical structure and reactivity. Further research and testing may uncover specific uses for this compound in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 225236-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,2,3 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 225236-02:
(8*2)+(7*2)+(6*5)+(5*2)+(4*3)+(3*6)+(2*0)+(1*2)=102
102 % 10 = 2
So 225236-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-15-13-7-3-2-5-11(13)9-14-10-12-6-4-8-16-12/h2-8,14H,9-10H2,1H3
225236-02-2Relevant articles and documents
Intra-molecular Diels-Alder reactions of citraconamic acids from furfurylamines and citraconic anhydride: Effects of substitution in the furan ring on regioselectivity
Murali, Rajappa,Surya Prakash Rao,Scheeren, Hans W
, p. 3165 - 3174 (2007/10/03)
Regioselectivity in the intra-molecular Diels-Alder (IMDA) reaction of furfurylcitraconamic acids derived from N-benzylfurfurylamines and citraconic anhydride can be controlled by substituents located in the furan ring and by reaction conditions. Reactions conducted under kinetic conditions resulted in cycloaddition products having methyl and aminomethylene substituent in 1,3-relationship whereas under thermodynamic conditions, excepting in the case of the 3-methylsulfanyl group, the products rearranged to more stable cycloadducts in which the substituents are in 1,2-relationship. Product formation can be explained on the basis of frontier orbital interactions and steric considerations.
