225236-01-1 Usage
General Description
FURAN-2-YLMETHYL-(2-METHYL-BENZYL)-AMINE is a chemical compound with the molecular formula C14H17N O. It is a derivative of benzylamine, containing a furan ring and a methyl group attached to the benzyl moiety. FURAN-2-YLMETHYL-(2-METHYL-BENZYL)-AMINE possesses a variety of potential applications, including in organic synthesis and pharmaceutical research. It may also serve as a building block for the development of new drugs and materials. However, given its structural features and potential reactivity, careful handling and proper safety precautions should be followed when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 225236-01-1 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 225236-01:
(8*2)+(7*2)+(6*5)+(5*2)+(4*3)+(3*6)+(2*0)+(1*1)=101
101 % 10 = 1
So 225236-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO/c1-11-5-2-3-6-12(11)9-14-10-13-7-4-8-15-13/h2-8,14H,9-10H2,1H3/p+1
225236-01-1Relevant 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.
