58520-04-0 Usage
Description
1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan, also known as 1,2-Di(4'-methoxyphenyl)ethylenediamine or 1,2-Bis(4-methoxyphenyl)ethylenediamine, is a chemical compound characterized by two 4'-methoxyphenyl groups attached to a central ethylenediamine backbone. This unique structure endows it with specific properties that make it a valuable asset in the fields of organic synthesis and medicinal chemistry.
Uses
Used in Organic Synthesis:
1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan is used as a building block in organic synthesis for the creation of complex molecules. Its versatile structure allows for the development of a wide range of compounds with diverse applications.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan serves as a key component in the development of new drugs and treatments. Its unique properties contribute to the design and synthesis of innovative therapeutic agents.
Used as a Reagent in Chemical Reactions:
1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan is utilized as a reagent to facilitate the formation of new carbon-nitrogen bonds in chemical reactions. This capability is crucial for advancing research and enhancing the synthesis of novel compounds in organic chemistry.
Used in Research:
The distinctive structure and properties of 1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan make it an indispensable tool for researchers and chemists. It aids in exploring new chemical pathways and contributes to the advancement of knowledge in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 58520-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,2 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58520-04:
(7*5)+(6*8)+(5*5)+(4*2)+(3*0)+(2*0)+(1*4)=120
120 % 10 = 0
So 58520-04-0 is a valid CAS Registry Number.
58520-04-0Relevant articles and documents
Syntheses of Families of Enantiopure and Diastereopure Cobalt Catalysts Derived from Trications of the Formula [Co(NH2CHArCHArNH2)3]3+
Ghosh, Subrata K.,Lewis, Kyle G.,Kumar, Anil,Gladysz, John A.
, p. 2304 - 2320 (2017/02/26)
Aerobic reactions of CoX2 (X = OAc, Cl) or Co(ClO4)2 with (S,S)-1,2-diphenylethylenediamine [(S,S)-dpen] in CH3OH, followed by HCl or HClO4 additions, give the diastereomeric lipophobic salts Λ-[Co((S
SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS
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Page/Page column 8, (2008/06/13)
A diamine of formula (I) is described, in which A is hydrogen or a saturated or unsaturated C1-C20 alkyl group or an aryl group; B is a substituted or unsubstituted C1-C20 alkyl, cycloalkyl, alkaryl, alkaryl or aryl group or an alkylamino group and at least one of X1, X2, Y1, Y2 or Z is a C1-C10 alkyl, cycloalkyl, alkaryl, aralkyl or alkoxy substituting group. The chiral diamine may be used to prepare catalysts suitable for use in transfer hydrogenation reactions.