87306-84-1 Usage
Uses
Used in Organic Chemistry:
2,2'-Dimethoxy-6-formylbiphenyl is used as a starting material for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of derivatives, making it an essential component in the development of new chemical entities.
Used in Material Science:
In the field of material science, 2,2'-Dimethoxy-6-formylbiphenyl is used as a building block for the development of new materials with specific properties. Its versatility in chemical reactions enables the creation of materials with tailored characteristics for various applications.
Used in Photoresponsive Materials:
2,2'-Dimethoxy-6-formylbiphenyl is used as a valuable tool in the research and development of photoresponsive materials. Its photophysical and photochemical properties make it suitable for applications in areas such as solar energy conversion, light-emitting diodes, and sensors.
Used in Therapeutic and Pharmaceutical Applications:
The potential biological activity of 2,2'-Dimethoxy-6-formylbiphenyl is currently being explored for its use in therapeutic and pharmaceutical applications. Its unique chemical structure may offer new opportunities for the development of novel drugs and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 87306-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,0 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87306-84:
(7*8)+(6*7)+(5*3)+(4*0)+(3*6)+(2*8)+(1*4)=151
151 % 10 = 1
So 87306-84-1 is a valid CAS Registry Number.
87306-84-1Relevant academic research and scientific papers
Nucleophilic aromatic substitution on aromatic aldimines
Flippin, Lee A.,Carter, David S.,Dubree, Nathan J. P.
, p. 3255 - 3258 (2007/10/02)
Ortho-methoxy-substituted benzaldimines derived from 3-amino-2,4-dimethylpentane undergo efficient nucleophilic aromatic substitution with typical organolithium reagents. The aldimine products can be hydrolyzed under mild conditions to provide ortho-alkyl or ortho-phenyl benzaldehyde derivatives.
Enantioselective Synthesis of 2,2',6-Trisubstituted Biphenyls
Meyers, A. I.,Himmelsbach, Richard J.
, p. 682 - 685 (2007/10/02)
A general procedure is described for the synthesis of chiral biphenyls via nucleophilic aromatic substitution of an o-methoxy group by an aryl Grignard reagent with an oxazoline as a chiral auxiliary.
Reductive Cleavage of Aryl Oxazolines to Benzaldehydes and Substituted Toluenes
Meyers, A. I.,Himmelsbach, Richard J.,Reuman, Michael
, p. 4053 - 4058 (2007/10/02)
Aryl oxazolines have been converted to their corresponding benzaldehydes and toluenes by several routes by passing through the intermediate amino alcohols.The transformations proceeded under mild conditions and were shown to be generally applicable to a variety of substitutions on the aromatic nucleus.
