6629-38-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(3,3-dimethylbicyclo[2.2.1]hept-2-yl)acetamide is used as a potential candidate for drug development due to its structural similarity to biologically active molecules, which may confer it with pharmacological properties that could be beneficial in the creation of new medications.
Used in Chemical Building Blocks:
In the chemical industry, 2-(3,3-dimethylbicyclo[2.2.1]hept-2-yl)acetamide is used as a chemical building block for the synthesis of more complex molecules, given its unique bicyclic structure and functional groups that can be further modified or utilized in the creation of novel compounds.
Further research is essential to explore the compound's potential pharmacological effects and to determine its practical applications across various fields, including but not limited to medicinal chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 6629-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6629-38:
(6*6)+(5*6)+(4*2)+(3*9)+(2*3)+(1*8)=115
115 % 10 = 5
So 6629-38-5 is a valid CAS Registry Number.
6629-38-5Relevant academic research and scientific papers
Ethylamine derivatives of cineole and norbornane
Mariani,Schenone
, p. 113 - 119 (2007/10/06)
Synthesis of 6 (2 aminoethyl) 1,3,3 trimethyl 2 oxabicyclo (2.2.2)octane (cineole 6 ethylamine) and 2 (2 aminoethyl) 3,3 dimethylbicyclo (2.2.1) heptane (3,3 dimethylnorbornane 2 ethylamine) and their unsaturated (2 aminoethylidene) analogs is described. 2 (2 Aminoethylidene) 3,3 dimethylbicyclo (2.2.1) heptane showed antiinflammatory and central stimulant activities in mouse; the cineole derivative, 6 (2 aminoethylidene) 1,3,3 trimethyl 2 oxabicyclo (2.2.2) octane, showed antiarrhythmic activity. 6 (Cyanomethylene) 1,3,3 trimethyl 2 oxabicyclo (2.2.2) octane, an intermediate to the synthesis of the cineole ethylamine derivatives, showed muscle relaxant activity.
