692257-58-2 Usage
Uses
Used in Pharmaceutical Research:
1-(3-bromphenyl)-1-propylamine is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structural properties and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Organic Synthesis:
1-(3-bromphenyl)-1-propylamine is used as a key intermediate in the preparation of complex organic molecules. Its versatility in forming different types of chemical bonds allows it to be a useful component in the creation of a wide range of organic compounds.
Used in Drug Development:
1-(3-bromphenyl)-1-propylamine is used as a starting material in the development of new drugs and medicinal compounds. Its potential applications in this field are due to its structural properties and reactivity, which can be harnessed to create novel therapeutic agents.
Used in Chemical Research:
1-(3-bromphenyl)-1-propylamine is used as a research tool in the study of chemical reactions and mechanisms. Its unique properties make it an interesting subject for understanding various aspects of chemical behavior and reactivity.
Used in Industrial Applications:
1-(3-bromphenyl)-1-propylamine may be used in various industrial applications, such as the production of specialty chemicals, agrochemicals, or other related products. Its specific use would depend on the requirements of the particular industry and the desired end product.
Check Digit Verification of cas no
The CAS Registry Mumber 692257-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,2,5 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 692257-58:
(8*6)+(7*9)+(6*2)+(5*2)+(4*5)+(3*7)+(2*5)+(1*8)=192
192 % 10 = 2
So 692257-58-2 is a valid CAS Registry Number.
692257-58-2Relevant academic research and scientific papers
SYNTHESIS OF CHIRAL AMINES
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Page/Page column 5, (2010/01/30)
The instant invention involves the enantioselective hydrogenation of isomeric N-H imines (N-unsubstituted) using a transition metal based catalyst modified with a chiral phosphine derivative to produce enantiomerically enriched chiral amines.
