91551-59-6 Usage
Uses
Used in Pharmaceutical Industry:
3-(2,6-DIMETHYLMORPHOLIN-4-YL)PROPAN-1-AMINE is utilized as a building block in organic synthesis for the development of new pharmaceuticals. Its unique structure and biological activities contribute to the creation of innovative drugs that can address various health concerns.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(2,6-DIMETHYLMORPHOLIN-4-YL)PROPAN-1-AMINE serves as an intermediate in the production of agrochemicals. Its antifungal, antibacterial, and antiviral properties make it a valuable component in developing effective solutions for crop protection and enhancement of agricultural yields.
Used in Materials Science:
3-(2,6-DIMETHYLMORPHOLIN-4-YL)PROPAN-1-AMINE has potential applications in materials science, where its chemical structure can be employed to engineer new materials with specific properties. This can lead to advancements in various industries, such as electronics, textiles, and construction.
Used as a Reagent in Chemical Reactions:
Due to its versatile chemical structure, 3-(2,6-DIMETHYLMORPHOLIN-4-YL)PROPAN-1-AMINE is also used as a reagent in various chemical reactions. It can facilitate or catalyze specific processes, enabling the synthesis of complex molecules and compounds for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 91551-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91551-59:
(7*9)+(6*1)+(5*5)+(4*5)+(3*1)+(2*5)+(1*9)=136
136 % 10 = 6
So 91551-59-6 is a valid CAS Registry Number.
91551-59-6Relevant academic research and scientific papers
A structure-activity relationship study of novel phenylacetamides which are sodium channel blockers
Roufos, Ioannis,Hays, Sheryl,Schwarz, Roy D.
, p. 1514 - 1520 (2007/10/03)
A structure-activity relationship study of a series of novel Na+ channel blockers, structurally related to N-[3-(2,6-dimethyl-1-piperidinyl)propyl]- α-phenylbenzeneacetamide (1, PD85639) is described. The diphenylacetic acid portion of the molecule was left unchanged throughout the study, while structural features in the amine portion and the amide alkyl linkage of the molecule were modified. The compounds were tested for inhibition of veratridine-stimulated Na+ influx in CHO cells expressing type IIA Na+ channels. Several derivatives show a trend toward more potent Na+ channel blockade activity with increasing lipophilicity of the amine portion of the molecule. The presence of a phenyl ring near the amine increases inhibitory potency. A three-carbon spacer between the amide and amine is optimal, and a secondary amide linkage is preferred.
