116006-20-3 Usage
Chemical composition
Contains a bromine atom, a hydroxyl group, a methoxy group, and an acetaldehyde moiety.
Usage
Commonly used as an intermediate in organic synthesis.
Industries involved
Particularly used in the production of pharmaceuticals and agrochemicals.
Potential applications
May have applications in the field of medicine and agriculture.
Reactive nature
Ability to form new chemical bonds.
Importance in research
Unique chemical composition may make it a valuable tool for research in organic chemistry and chemical engineering.
Structure and properties
Make it an important building block for the creation of new drugs and pesticides.
Check Digit Verification of cas no
The CAS Registry Mumber 116006-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116006-20:
(8*1)+(7*1)+(6*6)+(5*0)+(4*0)+(3*6)+(2*2)+(1*0)=73
73 % 10 = 3
So 116006-20-3 is a valid CAS Registry Number.
116006-20-3Relevant academic research and scientific papers
Total synthesis of linoxepin through a palladium-catalyzed domino reaction
Tietze, Lutz F.,Duefert, Svenia-C.,Clerc, Jér?me,Bischoff, Matthias,Maa?, Christian,Stalke, Dietmar
supporting information, p. 3191 - 3194 (2013/04/23)
Convergent and elegant: Linoxepin (see picture), a new lignan with an unusual oxepin moiety, has been synthesized in only 10 steps. The protecting-group-free total synthesis includes a palladium- catalyzed Sonogashira reaction and a domino carbopalladation/Heck reaction of an allylsilane.
Chemoenzymatic total synthesis of ent-neopinone and formal total synthesis of ent -codeinone from β-bromoethylbenzene
Duchek, Jan,Piercy, T. Graeme,Gilmet, Jacqueline,Hudlicky, Tomas
, p. 709 - 728 (2011/11/13)
Formal total synthesis of ent-codeinone and ent-codeine was accomplished via the total synthesis of ent-neopinone attained in 14 steps from β-bromoethylbenzene. The key steps included (i) enzymatic dihydroxylation of β-bromoethylbenzene with E. coli JM109
