13078-82-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-AMINOPHENYL)ETHYL AMINE 2HCL is used as an intermediate compound for the synthesis of Tyrosol and its transformation into Hordenine. This application is crucial in the development of pharmaceutical products, as Tyrosol and Hordenine have potential therapeutic properties and can be used in the treatment of various medical conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-(4-AMINOPHENYL)ETHYL AMINE 2HCL serves as a key building block for the creation of more complex molecules. Its unique structure allows it to be a versatile component in the synthesis of various organic compounds, contributing to the development of new materials and products across different industries.
Used in Research and Development:
2-(4-AMINOPHENYL)ETHYL AMINE 2HCL is also utilized in research and development laboratories for the study of its chemical properties and potential applications. Scientists and researchers use this compound to explore new reactions, develop novel synthesis methods, and investigate its potential uses in various fields, including pharmaceuticals, materials science, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 13078-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,7 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13078-82:
(7*1)+(6*3)+(5*0)+(4*7)+(3*8)+(2*8)+(1*2)=95
95 % 10 = 5
So 13078-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2.ClH/c9-6-5-7-1-3-8(10)4-2-7;/h1-4H,5-6,9-10H2;1H
13078-82-5Relevant articles and documents
Rapid Conventional and Microwave-Assisted Decarboxylation of L-Histidine and Other Amino Acids via Organocatalysis with R-Carvone under Superheated Conditions
Jackson, Douglas M.,Ashley, Robert L.,Brownfield, Callan B.,Morrison, Daniel R.,Morrison, Richard W.
, p. 2691 - 2700 (2015/12/18)
This article reports a new methodology taking advantage of superheated chemistry via either microwave or conventional heating for the facile decarboxylation of alpha amino acids using the recoverable organocatalyst, R-carvone. The decarboxylation of amino acids is an important synthetic route to biologically active amines, and traditional methods of amino acid decarboxylation are time consuming (taking up to several days in the case of L-histidine), are narrow in scope, and make use of toxic catalysts. Decarboxylations of amino acids including L-histidine occur in just minutes while replacing toxic catalysts with green catalyst, spearmint oil. Yields are comparable to or exceed previous methods and purification of product ammonium chloride salts is aided by an isomerization reaction of residual catalyst to phenolic carvacrol. The method has been shown to be effective for the decarboxylations of a range of natural, synthetic, and protected amino acids.
FRICTIONLESS MOLECULAR ROTARY MOTORS
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Page/Page column 33, (2010/02/17)
A rotaxane consisting of a cucurbituril and an uncharged guest molecule, having low or null affinity therebetween is provided as well as processes for providing the same. Various uses as energy converters (“frictionless” molecular motors), biochips and biosensors using the same are also provided.
