85553-44-2 Usage
Uses
Used in Organic Synthesis:
2-[3-(Bromomethyl)phenyl]thiophene is utilized as a key intermediate in organic synthesis for the production of various complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of compounds with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-[3-(Bromomethyl)phenyl]thiophene is employed as a building block for the development of new drugs. Its potential biological activities and structural features make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Medicinal Chemistry:
2-[3-(Bromomethyl)phenyl]thiophene is used as a starting material in medicinal chemistry for the exploration and development of new drugs. Its chemical properties and potential interactions with biological targets make it a valuable component in the creation of pharmaceutical compounds with specific therapeutic effects.
Used in Environmental and Health Safety:
As a brominated aromatic compound, 2-[3-(Bromomethyl)phenyl]thiophene requires careful handling and storage to prevent potential health hazards and environmental contamination. Proper management and disposal methods are essential to mitigate risks associated with its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 85553-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,5 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85553-44:
(7*8)+(6*5)+(5*5)+(4*5)+(3*3)+(2*4)+(1*4)=152
152 % 10 = 2
So 85553-44-2 is a valid CAS Registry Number.
85553-44-2Relevant academic research and scientific papers
New Methods of Formation of Meta-Substituted Aromatic Compounds
Adams, Julian,Belley, Michel
, p. 3878 - 3881 (2007/10/02)
The addition of organolithium reagents to the oxa tricyclic ketone 1 occurs stereospecifically to produce the corresponding tertiary carbinols 2a-d.When the alcohols 2a-d are treated with TiCl4, ring fragmentation and dehydration occur to produce good yields of 5,6-dihydrobenzaldehydes 3a-d.Oxidation of aldehydes 3a-d then leads to the corresponding meta-substituted benzaldehydes 4a-d.Alternatively, use of the Lewis acid Me2BBr did not stop at the dihydrobenzaldehyde stage.Tautomerization of the diene aldehydes 3a-d produced meta-substituted benzyl alcohols 7a-d or benzyl bromides 8a-d under prolonged reaction times.The addition of silica gel to the reactions accelerated the formation of the benzyl bromides.
Heterocyclic substituted benzyl alcohol, insecticidal ester derivatives, and intermediates
-
, (2008/06/13)
Disclosed and exemplified are insecticidal and acaricidal optionally substituted furylbenzyl, thienylbenzyl, pyrazinylbenzyl, or pyridinzylbenzyl esters of the pyrethroid acids, novel pyrethroid alcohols and other intermediates, and compositions, a method of use and a process for preparation of the esters.
