58520-04-0

Usage

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.

Upstream product

• 117106-36-2 d,l-1,2-diamino-1,2-bis(4-methoxyphenyl)ethane 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 91548-22-0 (S,S)-1,2-Bis(4-hydroxyphenyl)-1,2-ethanediamine 
• 787590-29-8 (1S,2S)-(-)-1,2-bis(tert-butoxycarbonylamino)-1,2-bis(4-hydroxyphenyl)ethane 
• 896155-78-5 (1S,2S)-(+)-1,2-bis(tert-butoxycarbonylamino)-1,2-bis(4-decyloxyphenyl)ethane 
• 787590-31-2 [1,2-bis-(4-benzyloxy-phenyl)-2-tert-butoxycarbonylamino-ethyl]-carbamic acid tert-butyl ester 
• 863117-83-3 {1,2-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-2-tert-butoxycarbonylamino-ethyl}-carbamic acid tert-butyl ester 
• 855309-78-3 [2-tert-butoxycarbonylamino-1-(4-hydroxy-phenyl)-2-(4-methoxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 855309-79-4 [2-[4-(4-{4-[1,2-bis-tert-butoxycarbonylamino-2-(4-methoxy-phenyl)-ethyl]-phenoxymethyl}-benzyloxy)-phenyl]-2-tert-butoxycarbonylamino-1-(4-methoxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 887924-07-4 (1S,2S)-N-p-toluenesulfonyl-1,2-di(4-methoxyphenyl)ethylenediamine 
• 1092654-41-5 C₂₃H₂₂N₂O₂ 
• 1619263-28-3 C₅₇H₅₄N₆O₆ 
• 1599484-91-9 C₃₈H₄₂N₄O₈S₂ 

Relevant academic research and scientific papers

Syntheses of Families of Enantiopure and Diastereopure Cobalt Catalysts Derived from Trications of the Formula [Co(NH2CHArCHArNH2)3]3+

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

TRANSITION METAL COMPLEXES FOR ENANTIOSELECTIVE CATALYSIS OF CARBON-CARBON, CARBON-HETEROATOM, AND CARBON-HYDROGEN BOND FORMING REACTIONS

In some embodiments, the present disclosure pertains to a compound, comprising a transition metal complex having the formula Φ-[Μ (x,y)-L1 (w,v)-L2 (t,u)-L3]p+An-mZ-p_m. In an embodiment of the present disclosure Φ may be A. In another embodiment Φ may be Δ. In some embodiments of the present disclosure, M is a transition metal. In a related embodiment, p is an integer corresponding to the oxidation state of M. In some embodiments of the present disclosure, each of x, y, w, v, t, and u independently comprise R. In other embodiments, each of x, y, w, v, t, and u independently comprise S. In an embodiment of the present disclosure, each of L1, L2, and L3 independently is a ligand comprising a substituted diamine. In some embodiments, An" comprises a lipophilic anion, where m is from 1 to 3, and where Z- comprises an optional second anion.

SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS

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.

Convenient Routes to Symmetrical Benzils and Chiral 1,2-Diaryl-1,2-diaminoethanes, Useful Controllers and Probes for Enantioselective Synthesis

Pathways for the diastereoselective preparation of chiral 1,2-diaryl-1,2-diaminoethanes from ArCOOH, ArCHO or ArBr are described.