809282-30-2 Usage
Description
(R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine is a chiral amine chemical compound with the molecular formula C17H25NO. It is characterized by its non-superimposable mirror image and is primarily utilized as a building block in the synthesis of pharmaceuticals and other organic compounds. (R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine features a 3-methoxyphenyl group and a N,N,2-trimethylpent-3-en-1-amine group, making it a versatile component in the development of drugs, research chemicals, and various biochemicals. Its applications extend to biochemistry, pharmaceuticals, and other domains of chemical research.
Uses
Used in Pharmaceutical Industry:
(R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine is used as a building block for the synthesis of various pharmaceuticals due to its unique structural properties. Its chiral nature allows for the creation of enantiomerically pure compounds, which can be crucial in the development of more effective and selective medications.
Used in Chemical Research:
In the field of chemical research, (R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine serves as an important compound for the development of new organic materials and the study of their properties. Its structural features make it a valuable tool for understanding the behavior of chiral molecules and their interactions with other compounds.
Used in Biochemical Applications:
(R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine is also utilized in biochemistry for the investigation of biological processes and the development of biochemical tools. Its unique structure can be employed to probe and manipulate biological systems, potentially leading to new insights and applications in the life sciences.
Overall, (R)-3-(3-Methoxyphenyl)-N,N,2-triMethylpent-3-en-1-aMine is a versatile and valuable compound with a wide range of applications across various industries, particularly in the development and synthesis of pharmaceuticals, as well as in chemical and biochemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 809282-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,8 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 809282-30:
(8*8)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*3)+(1*0)=172
172 % 10 = 2
So 809282-30-2 is a valid CAS Registry Number.
809282-30-2Relevant articles and documents
Process for Preparing a Substituted Dimethyl-(3-arylbutyl)amine Compound by Homogeneous Catalysis
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Page/Page column 10, (2009/03/07)
Compounds of the formula II can be hydrogenated to the corresponding butane derivatives in the presence of homogeneous cataslysts composed of metal salts or complexes containing metals selected from the group consisting of Rh, Ir, and Ru and preferably containing diphosphine ligands, with, in addition, excellent optical yields being achieved when one of R2 and R3 is not a hydrogen atom and the diphosphine ligand is chiral.
METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS
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Page/Page column 49-50, (2008/06/13)
The invention relates to a method for the dehydration of substituted 1-amino-3-aryl-butane-3-oil compounds for the production of substituted 3-aryl-butyl-amine compounds.
