56759-36-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(5-bromo-2-nitrophenyl)oxirane is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity allows it to participate in the formation of new carbon-carbon bonds and undergo various ring-opening reactions, which are essential in the development of new drugs.
Used in Agrochemical Industry:
2-(5-bromo-2-nitrophenyl)oxirane is used as a chemical intermediate in the production of agrochemicals. Its unique structure and reactivity contribute to the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals.
Used in Dye Industry:
2-(5-bromo-2-nitrophenyl)oxirane is used as a chemical intermediate in the synthesis of dyes. Its ability to undergo various chemical reactions enables the creation of a wide range of colored compounds, which are used in the production of textiles, paints, and other colored materials.
Used in Organic Synthesis:
2-(5-bromo-2-nitrophenyl)oxirane is used as a reagent in organic synthesis. Its reactive nature allows it to participate in various chemical reactions, such as ring-opening reactions, which are crucial in the formation of new carbon-carbon bonds and the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 56759-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,5 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56759-36:
(7*5)+(6*6)+(5*7)+(4*5)+(3*9)+(2*3)+(1*6)=165
165 % 10 = 5
So 56759-36-5 is a valid CAS Registry Number.
56759-36-5Relevant academic research and scientific papers
Agarwal, Hitesh K.,Janicek, Radoslav,Chi, San-Hui,Perry, Joseph W.,Niggli, Ernst,Ellis-Davies, Graham C. R.
, p. 3687 - 3693 (2016)
We have designed a nitroaromatic photochemical protecting group that absorbs visible light in the violet-blue range. The chromophore is a dinitro derivative of bisstyrylthiophene (or BIST) that absorbs light very effectively (ε440 = 66,000 M-1 cm-1 and two-photon cross section of 350 GM at 775 nm). We developed a "caged calcium" molecule by conjugation of BIST to a Ca2+ chelator that upon laser flash photolysis rapidly releases Ca2+ in 2+, was delivered into acutely isolated mouse cardiac myocytes, where either one- and two-photon uncaging of Ca2+ induced highly local or cell-wide physiological Ca2+ signaling events.
