67171-89-5 Usage
Classification
Lactam
Belongs to the class of lactams, which are cyclic amines with an oxygen atom in the ring.
Structure
Long-chain, saturated lactam
Features a long carbon chain and a saturated carbon backbone, providing stability and rigidity.
Side chain
2-Cyanoethylamino group
Contains a 2-cyanoethylamino group in its side chain, which contributes to its unique properties and potential applications.
Potential applications
Organic synthesis and materials science
Can be used as a monomer for the synthesis of polymers with specific properties, making it valuable in the fields of organic synthesis and materials science.
Polymer properties
High tensile strength and flexibility
The polymers synthesized from 13-Aza-16-[(2-cyanoethyl)amino]hexadecanoic acid lactam may exhibit high tensile strength and flexibility, making them suitable for various applications.
Pharmaceutical applications
Under investigation
Further research is needed to determine the potential medical uses of 13-Aza-16-[(2-cyanoethyl)amino]hexadecanoic acid lactam.
Check Digit Verification of cas no
The CAS Registry Mumber 67171-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67171-89:
(7*6)+(6*7)+(5*1)+(4*7)+(3*1)+(2*8)+(1*9)=145
145 % 10 = 5
So 67171-89-5 is a valid CAS Registry Number.
67171-89-5Relevant academic research and scientific papers
Transamidation Reactions. Part 11) N-Substituted 3-Aminopropanenitriles and 2-Aminoacetonitriles as Schiff-Base Equivalents
Askitoglu, Elefteria,Guggisberg, Armin,Hesse, Manfred
, p. 750 - 759 (2007/10/02)
In presence of a strong base, the 13-membered cyclic compound 3 yielded, by loss of acetonitrile or its equivalent, the bicyclic product 5 instead of the 17-membered compound 4 as expected (Scheme 2).Investigation of model compounds (Scheme 4) and of model reactions (Schemes 5 and 6) led to the conclusion that the reaction proceeds via an intermediate formaldehyde imine; a Schiff base, e. g. 3b (Scheme 5), which reacts intra- and intermolecularly with a nucleophile to form a Mannich-type product.It seems to be a general principle that N-substituted 3-aminopropanenitrile and 2-aminoacetonitrile derivatives behave in the presence of a strong base as Schiff-base equivalents (Scheme 5 and 6).
Amidine als Zwischenprodukte bei Umamidierungsreaktionen
Heidelberger, Christian,Guggisberg, Armin,Stephanou, Euripides,Hesse, Manfred
, p. 399 - 406 (2007/10/02)
By loss of water in the presence of p-toluenesulfonic acid/xylol N-aminoalkyl-lactames form bicyclic amidines.The corresponding N-alkylaminoalkyl-lactames react to bicyclic amidinium salts or to transamidated products, ring-enlarged by the N-alkylamino re
