1042-91-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
2,3-diazabicyclo[2.2.1]hept-5-ene-2,3-diylbis(phenylmethanone) is used as an organic base in various chemical reactions for the synthesis of pharmaceuticals and agrochemicals. Its ability to participate in a wide range of organic reactions contributes to its utility in creating complex organic molecules, enhancing the development of new drugs and agricultural products.
Used in Organic Synthesis as a Catalyst or Intermediate:
In the field of organic synthesis, 2,3-diazabicyclo[2.2.1]hept-5-ene-2,3-diylbis(phenylmethanone) is utilized as both a catalyst and an intermediate. Its high stability and low toxicity make it an ideal candidate for facilitating various chemical reactions, thereby improving the efficiency and effectiveness of organic synthesis processes.
Used in Chemical Research and Development:
2,3-diazabicyclo[2.2.1]hept-5-ene-2,3-diylbis(phenylmethanone) is also employed in chemical research and development due to its versatility and valuable properties. It serves as a key component in the exploration of new chemical reactions and the development of innovative synthetic pathways, further expanding the horizons of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1042-91-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1042-91:
(6*1)+(5*0)+(4*4)+(3*2)+(2*9)+(1*1)=47
47 % 10 = 7
So 1042-91-7 is a valid CAS Registry Number.
1042-91-7Relevant academic research and scientific papers
Stereospecific synthesis of cyclic hydrazoacetic acids and meso- diaminodicarboxylic acids
Arakawa, Yasushi,Goto, Takahiro,Kawase, Kazuya,Yoshifuji, Shigeyuki
, p. 674 - 680 (2007/10/03)
The hetero Diels-Alder adducts 6a - d derived from azodibenzoyl and cyclic dienes were oxidized by ruthenium tetroxide and transformed into meso- diaminodicarboxylic acids 12a - d via the new cyclic hydrazoacetic acids 9a - d.
