380641-63-4 Usage
Uses
Used in Pharmaceutical Research:
1-(2-methoxyphenyl)-1H-benzo[d]imidazol-5-amine is used as a research compound for exploring its potential in medicinal chemistry. Its structural resemblance to biologically active molecules suggests that it could be a valuable tool in the development of new therapeutic agents for various diseases.
Used in Drug Development:
In the pharmaceutical industry, 1-(2-methoxyphenyl)-1H-benzo[d]imidazol-5-amine is used as a starting point for designing novel drug candidates. Its chemical structure and properties allow researchers to investigate structure-activity relationships, which can lead to the creation of more effective and targeted treatments for a range of medical conditions.
Used in Structure-Activity Relationship Studies:
1-(2-methoxyphenyl)-1H-benzo[d]imidazol-5-amine is utilized as a key compound in structure-activity relationship studies. These studies are crucial for understanding how the molecular structure of a compound influences its biological activity, which can inform the design of more potent and selective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 380641-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,6,4 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 380641-63:
(8*3)+(7*8)+(6*0)+(5*6)+(4*4)+(3*1)+(2*6)+(1*3)=144
144 % 10 = 4
So 380641-63-4 is a valid CAS Registry Number.
380641-63-4Relevant academic research and scientific papers
SMALL MOLECULE COMPOUNDS FOR STEM CELL DIFFERENTIATION
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Page/Page column 59; 60, (2010/04/25)
Methods and small molecule compounds for stem cell differentiation are provided. One example of a class of compounds that may be used is represented by the compound having the structure IA or IB in the form of free base or a pharmaceutically acceptable salt, hydrate, solvate or N-oxide thereof. R1 is independently hydrogen or (C1-C6)alkyl; R2 is independently hydrogen, (C1-C6)alkyl, aryl, or heteroaryl; R2' is independently hydrogen, (C1-C6)alkyl, CF3 or C2F5; R3 is independently (C1-C6)alkyl, aryl, 2-tetrahydrofuryhnethyl, an aliphatic tertiary amine, or 4-methoxybenzyl; or R2 and R3 may be joined together to form a 5 or 6 member ring lactone; R4 is independently hydrogen, (C1-C6)alkyl, a 2- or 4-R5-substituted aromatic ring selected from a 4-R5-phenyl or a 2-R5-5-pyridyl, aryl, heteroaryl, aliphatic tertiary amine or halogen; and R5, R5', R6, R6', R7, R7' are each independently hydrogen, (C1-C6)alkyl, aryl, optionally substituted phenyl, heteroaryl, a heterocyclic ring, an aliphatic tertiary amine, or halogen.
