82040-74-2 Usage
Type of compound
Nitroaromatic compound
Structural features
Bromine atom
Two methoxy groups
Benzene ring
(E)-2-nitroethenyl group
Uses
Precursor in the synthesis of pharmaceuticals
Precursor in the synthesis of organic compounds
Potential building block for new materials and research chemicals
Physical state
Yellow crystalline solid
Molecular weight
289.10 g/mol
Hazard classification
Hazardous material
Safety measures
Special handling and storage precautions required
Potential risks
Toxicity and reactivity
Check Digit Verification of cas no
The CAS Registry Mumber 82040-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82040-74:
(7*8)+(6*2)+(5*0)+(4*4)+(3*0)+(2*7)+(1*4)=102
102 % 10 = 2
So 82040-74-2 is a valid CAS Registry Number.
82040-74-2Relevant articles and documents
Synthesis of 3-arylindole derivatives from nitroalkane precursors
Huang, Chia-Yu,Kuo, Chun-Wei,Konala, Ashok,Yang, Tang-Hao,Lin, Lyu,Chen, Yu-Wen,Kavala, Veerababurao,Yao, Ching-Fa
, p. 96049 - 96056 (2016/10/25)
3-Arylindole derivatives were synthesized by Cu(i) catalysed intramolecular Ullmann coupling of 2-bromoarylaminoalkanes. 2-Bromoarylaminoalkanes were synthesized from 2-bromoarylnitroalkanes, which in turn prepared through AlCl3-mediated Friede
An intramolecular aryne cycloaddition approach to phenanthrene alkaloids
Estevez,Estevez,Castedo
, p. 6883 - 6884 (2007/10/02)
A new synthesis of phenanthrene alkaloids which is based on the intramolecular Diels-Alder reaction between a styrene and an aryne is described.