72912-33-5 Usage
General Description
1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene is a chemical compound with the molecular formula C12H17BrO2. It is a white solid with a molecular weight of 281.16 g/mol. 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene is used in organic synthesis and pharmaceutical research as a building block for the synthesis of biologically active molecules. It contains a bromoethyl group and a methoxybenzene group, making it a versatile molecule for the modification of other organic compounds. The presence of the 1,1-dimethylethoxy group also makes it more stable and less prone to degradation, making it an ideal reagent for certain chemical reactions. Overall, this compound has potential applications in the pharmaceutical and chemical industries due to its reactivity and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 72912-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72912-33:
(7*7)+(6*2)+(5*9)+(4*1)+(3*2)+(2*3)+(1*3)=125
125 % 10 = 5
So 72912-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H19BrO2/c1-13(2,3)16-12(9-14)10-5-7-11(15-4)8-6-10/h5-8,12H,9H2,1-4H3
72912-33-5Relevant articles and documents
Electrochemical Alkoxyhalogenation of Alkenes with Organohalides as the Halide Sources via Dehalogenation
Li, Jin-Heng,Li, Yang,Luo, Mu-Jia,Song, Ren-Jie,Zhang, Ting-Ting
supporting information, p. 7250 - 7254 (2020/10/05)
A general, ideal atom utilization electrochemical technology to enable alkene alkoxyhalogenation and organohalide dehalogenation in one pot is presented. This technology is highlighted by convergent strategy integrating several reactions, such as alkene alkoxyhalogenation, organohalide dehalogenation, and dehalogenation deuteration. Experimental data suggest that alkenes have the lowest oxidation potential, which lead to anodic conversion of the C═C bond to the radical cation intermediates, and cathodic transformations of organohalides, including alkyl and aryl halides, as the nucleophilic halogen sources.
Synthesis and renal vasodilator activity of some dopamine agonist 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diols: Halogen and methyl analogues of fenoldopam
Weinstock,Ladd,Wilson,Brush,Yim,Gallagher Jr.,McCarthy,Silvestri,Sarau,Flaim
, p. 2315 - 2325 (2007/10/02)
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