188049-29-8 Usage
General Description
"(2E)-N-ethyl-3-phenylprop-2-en-1-amine" is a chemical compound with the molecular formula C11H15N, and a molar mass of 161.24 g/mol. It is also known as N-ethyl-3-phenyl-2-propen-1-amine and is classified as an amine, which is a derivative of ammonia where one or more hydrogen atoms are replaced by organic groups. (2E)-N-ethyl-3-phenylprop-2-en-1-amine is a secondary amine, meaning it has two organic groups attached to the nitrogen atom. It is commonly used in organic synthesis and pharmaceutical research, and its structural properties make it an important building block for the production of various chemicals and pharmaceuticals. Additionally, its structure contains a double bond, giving it the potential for interesting chemical reactivity and applications in various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 188049-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,0,4 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 188049-29:
(8*1)+(7*8)+(6*8)+(5*0)+(4*4)+(3*9)+(2*2)+(1*9)=168
168 % 10 = 8
So 188049-29-8 is a valid CAS Registry Number.
188049-29-8Relevant articles and documents
Ene reactions of alkynes for the stereoselective synthesis of allylamines
Ofial,Mayr
, p. 143 - 145 (1997)
Counterion in control! When complex anions with low nuclephilicity are used, a previously unknown ene reaction of iminium ions and alkynes occurs [Eq. (a)], which provides straihtforward stereo- and regioselective access to substituted allylamines.
