50764-59-5 Usage
Uses
Used in Analytical Chemistry:
MESO-1,2-BIS(P-TOLYL)ETHYLENEDIAMINE is used as a fluorogenic reagent for detecting and quantifying reducing carbohydrates. Its application in this field is due to its ability to react with reducing sugars, leading to the generation of a fluorescent signal that can be measured and analyzed.
Used in Pharmaceutical Research:
In the pharmaceutical industry, MESO-1,2-BIS(P-TOLYL)ETHYLENEDIAMINE is used as a key intermediate in the synthesis of various drugs and drug candidates. Its unique chemical properties make it a valuable component in the development of new therapeutic agents.
Used in Material Science:
MESO-1,2-BIS(P-TOLYL)ETHYLENEDIAMINE is also utilized in the field of material science, particularly in the development of novel materials with specific properties. Its chemical structure allows for the creation of new compounds with potential applications in various industries.
Used in Environmental Science:
In environmental science, MESO-1,2-BIS(P-TOLYL)ETHYLENEDIAMINE is employed as a tool for detecting and monitoring the presence of reducing carbohydrates in various environmental samples. This helps in understanding the role of these carbohydrates in ecological processes and their impact on the environment.
Used in Food Industry:
In the food industry, MESO-1,2-BIS(P-TOLYL)ETHYLENEDIAMINE is used as an analytical tool for determining the sugar content in various food products. Its ability to detect reducing sugars makes it a valuable asset in ensuring the quality and safety of food items.
Check Digit Verification of cas no
The CAS Registry Mumber 50764-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,6 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50764-59:
(7*5)+(6*0)+(5*7)+(4*6)+(3*4)+(2*5)+(1*9)=125
125 % 10 = 5
So 50764-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N2/c1-11-3-7-13(8-4-11)15(17)16(18)14-9-5-12(2)6-10-14/h3-10,15-16H,17-18H2,1-2H3/p+2/t15-,16+
50764-59-5Relevant academic research and scientific papers
Lipase-catalyzed desymmetrization of meso-1,2-diaryl-1,2-diaminoethanes
Mendez-Sanchez, Daniel,Rios-Lombardia, Nicolas,Garcia-Granda, Santiago,Montejo-Bernardo, Jose,Fernandez-Gonzalez, Alfonso,Gotor, Vicente,Gotor-Fernandez, Vicente
, p. 381 - 386 (2014/04/03)
The synthesis and enzyme-catalyzed desymmetrization of meso-1,2-diaryl-1,2- diaminoethanes have been investigated. A family of aromatic meso-1,2-diamines, containing different substitution patterns in the aromatic ring, was first prepared and then desymmetrized enantioselectively using lipases as biocatalysts. Selective alkoxycarbonylation of one of the amino groups was achieved using allyl carbonates, isolating the corresponding allyl monocarbamates with moderate to high enantiomeric excess at 45 C. Candida antarctica lipase types A (CAL-A) and B (CAL-B) displayed the best activities and stereopreferences, with a dramatic influence being observed depending on the diamine structure. Non substituted and para-substituted aryldiamines led to the formation of allyl carbamates with good enantiomeric excess, using CAL-A for the less hindered substrates and CAL-B for the more hindered ones. On the other hand meta- and ortho-derivatives afforded low or negligible conversions and selectivities, respectively.
Reductive coupling of aromatic oxims and azines to 1,2-diamines using Zn-MsOH or Zn-TiCl4
Kise, Naoki,Ueda, Nasuo
, p. 2365 - 2368 (2007/10/03)
The reduction of aromatic aldoxims and azines with Zn in the presence of MsOH or TiCl4 afforded N,N′-unsubstituted 1,2-diamines in one-step. The reductive coupling with Zn-MsOH gave meso 1,2-diamines selectively, whereas dl 1,2-diamines were fo
