64642-17-7 Usage
Uses
Due to the limited information available in the public domain regarding the specific applications and industrial use of 2-(Methylamino)-N-(4-methylphenyl)acetamide hydrochloride, the following uses are speculative and based on its chemical structure and potential reactivity:
Used in Chemical Synthesis:
2-(Methylamino)-N-(4-methylphenyl)acetamide hydrochloride is used as a reagent for the synthesis of various organic compounds. Its ability to act as both a nucleophile and an electrophile makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-(Methylamino)-N-(4-methylphenyl)acetamide hydrochloride may be used as a building block for the development of new drugs. Its structural features could be exploited to design molecules with specific biological activities, such as analgesics, anti-inflammatory agents, or other therapeutic compounds.
Used in Material Science:
2-(Methylamino)-N-(4-methylphenyl)acetamide hydrochloride could be employed in the development of new materials with unique properties. Its potential to participate in various chemical reactions may allow for the creation of novel polymers, coatings, or other materials with specific characteristics for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 64642-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,4 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64642-17:
(7*6)+(6*4)+(5*6)+(4*4)+(3*2)+(2*1)+(1*7)=127
127 % 10 = 7
So 64642-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O/c1-8-3-5-9(6-4-8)12-10(13)7-11-2/h3-6,11H,7H2,1-2H3,(H,12,13)/p+1
64642-17-7Relevant academic research and scientific papers
Structure-Based Design, Synthesis, and Antifungal Activity of New Triazole Derivatives
Sheng, Chunquan,Che, Xiaoying,Wang, Wenya,Wang, Shengzheng,Cao, Yongbing,Yao, Jianzhong,Miao, Zhenyuan,Zhang, Wannian
scheme or table, p. 309 - 313 (2012/05/05)
A series of new antifungal triazole derivatives with phenylacetamide side chain were rational designed and synthesized on the basis of the structural information of lanosterol 14-demethylase (CYP51). In vitro antifungal activity assay indicated that several compounds showed higher activity than fluconazole. Especially, compound 8h showed excellent inhibitory activity against Candida albicans and Cryptococcus neoformans (MIC=0.0156μg/mL), suggesting that it is a promising lead for the development of novel antifungal agents. The binding mode of compound 8h was investigated by flexible molecular docking. It interacted with CACYP51 through hydrophobic and van der Waals interactions. A series of phenylacetamide-containing new azoles with good in vitro antifungal activity were rationally designed and synthesized.
