69780-80-9 Usage
Uses
Used in Pharmaceutical Industry:
(2E,6E)-N,N-bis(1,3-benzodioxol-5-ylmethyl)-3,7,11-trimethyldodeca-2,6,10-trien-1-amine is used as a pharmaceutical intermediate for the synthesis of various drugs. Its complex structure and multiple functional groups make it a promising candidate for the development of new therapeutic agents.
Used in Chemical Research:
(2E,6E)-N,N-bis(1,3-benzodioxol-5-ylmethyl)-3,7,11-trimethyldodeca-2,6,10-trien-1-amine is also used in chemical research for studying the properties and reactivity of complex organic molecules. Its unique structure and functional groups provide opportunities for investigating various chemical reactions and mechanisms.
Used in Material Science:
(2E,6E)-N,N-bis(1,3-benzodioxol-5-ylmethyl)-3,7,11-trimethyldodeca-2,6,10-trien-1-amine may have potential applications in material science, particularly in the development of new materials with specific properties. Its aromatic ring structures and functional groups could contribute to the creation of novel materials with unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 69780-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,8 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69780-80:
(7*6)+(6*9)+(5*7)+(4*8)+(3*0)+(2*8)+(1*0)=179
179 % 10 = 9
So 69780-80-9 is a valid CAS Registry Number.
69780-80-9Relevant academic research and scientific papers
Non anticholinergic gastric acid secretion inhibitors. New piperazine and related derivatives
Tricerri,Elitropi,Panto,et al.
, p. 555 - 562 (2007/10/08)
Some of the new piperazine derived compounds exhibited interesting gastric antisecretory properties without anticholinergic action. 1 Piperonyl 4 (3,7,11 trimethyl 2,6,10 dodecatrienyl) piperazine was the most active as an antisecretory agent in rat. Some analogous compounds, with the piperazine ring replaced by other heterocyclic or acyclic amines, were also prepared. Structure activity relationships are discussed.
