247907-32-0 Usage
Uses
Used in Organic Synthesis:
N'-(2-fluoro-benzyl)-N,N-dimethyl-propane-1,3-diamine is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and functional groups allow for a wide range of reactions and the formation of diverse chemical products.
Used in Pharmaceutical Intermediates:
In the pharmaceutical industry, N'-(2-fluoro-benzyl)-N,N-dimethyl-propane-1,3-diamine is used as a key intermediate in the development of new drugs. Its chemical properties make it a promising candidate for the synthesis of various medicinal compounds, potentially leading to the discovery of novel therapeutic agents.
Used in Medicinal Chemistry:
N'-(2-fluoro-benzyl)-N,N-dimethyl-propane-1,3-diamine is utilized in medicinal chemistry for the design and synthesis of bioactive molecules. Its fluoro-benzyl group and amine functionalities can be exploited to create compounds with specific biological activities, targeting various diseases and medical conditions.
Used in Drug Development:
N'-(2-fluoro-benzyl)-N,N-dimethyl-propane-1,3-diamine plays a crucial role in drug development, as it can be employed to develop new pharmaceuticals with improved efficacy, safety, and selectivity. Its unique structural features make it an attractive starting point for the design of innovative drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 247907-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,9,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 247907-32:
(8*2)+(7*4)+(6*7)+(5*9)+(4*0)+(3*7)+(2*3)+(1*2)=160
160 % 10 = 0
So 247907-32-0 is a valid CAS Registry Number.
247907-32-0Relevant academic research and scientific papers
Hendrix, James A.,Stefany, David W.
, p. 6749 - 6752 (1999)
A mild reduction of ortho-fluoro benzamides was discovered using LAH. The reaction proceeds cleanly and in moderate yields. The scope of the reaction is explored and a mechanism is proposed. A two carbon spacer between the amide and a 3°amine is optimal for this chelation controlled reaction.
