142602-43-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(Benzyloxy)-4-broMobenzaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable precursor for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Benzyloxy)-4-broMobenzaldehyde is utilized as a starting material for the production of various agrochemicals, including pesticides and herbicides. Its chemical properties allow for the creation of effective compounds that can protect crops from pests and diseases.
Used in Organic Synthesis:
2-(Benzyloxy)-4-broMobenzaldehyde is also employed in organic synthesis for the preparation of a wide range of organic compounds. Its versatility as a building block enables the synthesis of various target molecules with diverse applications in different industries.
Overall, 2-(Benzyloxy)-4-broMobenzaldehyde is a versatile chemical compound with significant applications in the pharmaceutical, agrochemical, and organic synthesis industries. Its unique structure and properties make it an essential precursor for the development of new and innovative products with potential benefits in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 142602-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,6,0 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142602-43:
(8*1)+(7*4)+(6*2)+(5*6)+(4*0)+(3*2)+(2*4)+(1*3)=95
95 % 10 = 5
So 142602-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H11BrO2/c15-13-7-6-12(9-16)14(8-13)17-10-11-4-2-1-3-5-11/h1-9H,10H2
142602-43-5Relevant academic research and scientific papers
Copper-Catalyzed Asymmetric Diyne Cyclization via [1,2]-Stevens-Type Rearrangement for the Synthesis of Chiral Chromeno[3,4-c]pyrroles
Hong, Feng-Lin,Hong, Pan,Lu, Xin,Shi, Chong-Yang,Ye, Long-Wu,Zhai, Tong-Yi,Zhu, Xin-Qi
supporting information, (2021/12/27)
Here, we report a copper-catalyzed asymmetric cascade cyclization/[1,2]-Stevens-type rearrangement via a non-diazo approach, leading to the practical and atom-economic assembly of various valuable chiral chromeno[3,4-c]pyrroles bearing a quaternary carbon
Total synthesis of exiguamines A and B inspired by catecholamine chemistry
Sofiyev, Vladimir,Lumb, Jean-Philip,Volgraf, Matthew,Trauner, Dirk
scheme or table, p. 4999 - 5005 (2012/06/04)
The evolution of a total synthesis of the exiguamines, two structurally unusual natural products that are highly active inhibitors of indolamine-2,3-dioxygenase (IDO), is described. The ultimately successful strategy involves advanced cross-coupling methodology and features a potentially biosynthetic tautomerization/electrocyclization cascade reaction that forms two heterocycles and installs a quaternary ammonium ion in a single synthetic operation. Copyright
PROCESSES FOR PRODUCTION OF 4-BIPHENYLYAZETIDIN-2-ONES
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Page/Page column 42; 45; 54; 56-57, (2008/12/05)
The present invention relates to processes for the production of 4-biphenylylazetidin-2-one derivatives of formula (I).
DIPHENYLHETEROCYCLE CHOLESTEROL ABSORPTION INHIBITORS
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Page/Page column 275-276, (2008/06/13)
Various azetidinone, pyrrolidine, imidazolidine, and oxazolidine derivatives are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.
