41727-47-3 Usage
Description
METHYL 3,5-DIBROMO-4-HYDROXYBENZOATE is an organic compound that serves as an important intermediate in the synthesis of various chemical compounds. It is characterized by the presence of a methyl group, two bromine atoms, and a hydroxyl group attached to a benzene ring.
Uses
Used in Chemical Synthesis:
METHYL 3,5-DIBROMO-4-HYDROXYBENZOATE is used as a chemical intermediate for the production of 4-hydroxy-3,5-di-pyridin-2-yl-benzoic acid methyl ester. This synthesis process typically occurs at a temperature range of 90-100°C, allowing for the formation of the desired compound with specific properties and applications.
While the provided materials do not specify the exact applications of the final product, 4-hydroxy-3,5-di-pyridin-2-yl-benzoic acid methyl ester, it can be inferred that this compound may have potential uses in various industries such as pharmaceuticals, materials science, or as a specialty chemical. Further research and development would be necessary to explore the specific applications and benefits of this synthesized compound.
Check Digit Verification of cas no
The CAS Registry Mumber 41727-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41727-47:
(7*4)+(6*1)+(5*7)+(4*2)+(3*7)+(2*4)+(1*7)=113
113 % 10 = 3
So 41727-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Br2O3/c1-13-8(12)4-2-5(9)7(11)6(10)3-4/h2-3,11H,1H3
41727-47-3Relevant articles and documents
A chemical probe for the estrogen receptor: Synthesis of the 3H-isotopomer of raloxifene
Dodge,Stocksdale,Jones
, p. 43 - 49 (1995)
Radiolabelled raloxifene (LY156758) has been prepared by tritium gas hydrogenolysis of a 3-aroyl-bis-brominated precursor. The requisite halogenated intermediate was accessed by regioselective aroylation of benzothiophene 6 with the acid chloride of 3,5-dibromo-4-[2-(1-piperdinyl)ethoxy]benzoic acid (5). Selective deprotection of the aryl methyl ethers in the presence of the ethoxy side-chain followed by palladium catalyzed halogen-tritium exchange provided the target compound with a specific activity of 30.1 Ci/mmol.
A strategy for position-selective epoxidation of polyprenols
Gnanadesikan, Vijay,Corey
supporting information; experimental part, p. 8089 - 8093 (2009/02/01)
An effective strategy has been developed for the efficient site-selective epoxidation of poylolefinic isoprenoid alcohols, based on the use of an internal control element for intramolecular reaction. The approach is illustrated by application to a series of polyisoprenoid alcohols (polyprenols) at substrate concentration of 0.5 mM. With polyprenol substrates having the hydroxyl function at one terminus, the internal epoxidation can be directed at the double bond of the polyprenol, which is either four or five away from the terminal hydroxyprenyl subunit.
A New Bromination Method for Phenols and Anisoles: NBS/HBF4*Et2O in CH3CN
Oberhauser, Thomas
, p. 4504 - 4506 (2007/10/03)
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