29622-29-5 Usage
Uses
Used in Pharmaceutical Research:
N-(2,6-Dimethylphenyl)-2-[(5-chloropentyl)methylamino]acetamide is used as a research compound for exploring its bioactivity and potential medicinal properties. Its unique structure may contribute to the development of new therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, N-(2,6-Dimethylphenyl)-2-[(5-chloropentyl)methylamino]acetamide is utilized as a lead compound in drug discovery processes. Its chemical properties may be optimized to create effective treatments for various medical conditions.
Used in Chemical Synthesis:
N-(2,6-Dimethylphenyl)-2-[(5-chloropentyl)methylamino]acetamide may also serve as an intermediate in the synthesis of other complex organic molecules, contributing to the advancement of chemical research and the creation of novel materials or pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 29622-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29622-29:
(7*2)+(6*9)+(5*6)+(4*2)+(3*2)+(2*2)+(1*9)=125
125 % 10 = 5
So 29622-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H25ClN2O/c1-13-8-7-9-14(2)16(13)18-15(20)12-19(3)11-6-4-5-10-17/h7-9H,4-6,10-12H2,1-3H3,(H,18,20)
29622-29-5Relevant academic research and scientific papers
Cyclizing compounds. 3. Local anesthetic action of N (ω haloalkyl) N methylaminoaceto 2,6 xylidides
Ross,Sandberg,Akerman,Domeij,Stening,Svensson
, p. 787 - 790 (2007/10/06)
A series of N (ω chloroalkyl) N methylaminoaceto 2,6 xylidides which are able to cyclize to quaternary ammonium derivates was synthesized and examined for local anesthetic action. As reference compounds the corresponding series of N alkylamine derivates were synthesized and tested. In both series of compounds the duration of anesthesia was prolonged by increasing the size of the side chain. In the N alkylamine series an optimal effect was obtained for the N hexylamine derivate. The duration of anesthesia produced by the cyclizing compounds in the sciatic nerve test in vivo was somewhat shorter than that for the noncyclizing compounds. The observation that the N 4 chlorobutyl derivate produced a longer block than the 5 chloropentylamine in this test indicates that the quaternary compounds formed may contribute to the duration of anesthesia.
