934492-69-0 Usage
Structure
1-(dibromomethyl)-3,5-dimethoxybenzene
It is a derivative of benzene with a dibromomethyl group (Br-CH2-Br) at the 1st position, and methoxy groups (-OCH3) at the 3rd and 5th positions.
Functional groups
Dibromomethyl, methoxy
The dibromomethyl group is a bromine-containing functional group, while the methoxy groups are oxygen-containing functional groups.
Chemical class
Aromatic compound
It belongs to the class of aromatic compounds due to the presence of a benzene ring.
Application
Organic synthesis, reagent in chemical research
The compound is used in the synthesis of various organic compounds and serves as a reagent in chemical research.
Hazardous properties
Potential irritant, harmful to aquatic organisms
It is a potential irritant to the skin, eyes, and respiratory system, and may have harmful effects on aquatic organisms.
Safety precautions
Handle with caution, proper disposal
It is important to handle 1-(dibromomethyl)-3,5-dimethoxybenzene with care and dispose of it properly to minimize environmental impact.
Environmental impact
Should be handled and disposed of properly
Due to its potential harmful effects on aquatic organisms, it is crucial to manage its use and disposal responsibly to protect the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 934492-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,4,9 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 934492-69:
(8*9)+(7*3)+(6*4)+(5*4)+(4*9)+(3*2)+(2*6)+(1*9)=200
200 % 10 = 0
So 934492-69-0 is a valid CAS Registry Number.
934492-69-0Relevant academic research and scientific papers
TETRACYCLIC INDOLE DERIVATIVES FOR TREATING HEPATITIS C VIRUS INFECTION
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Page/Page column 188-189, (2012/04/17)
Tetracyclic indole derivatives of formula (I), pharmaceutically acceptable salts and the pharmaceutical compositions thereof are provided, wherein A, A', G, R1, R15, U, V, V, W, W, X, X', Y, Y' are as defined in the invention. Use of these derivatives for treating hepatitis C virus (HCV) infection is also provided.
Couplings of benzylic halides mediated by titanocene chloride: Synthesis of bibenzyl derivatives
Barrero, Alejandro F.,Herrador, M. Mar,Del Moral, Jose F. Quilez,Arteaga, Pilar,Akssira, Mohammed,El Hanbali, Fadwa,Arteaga, Jesus F.,Dieguez, Horacio R.,Sanchez, Elena M.
, p. 2251 - 2254 (2007/10/03)
Titanocene monochloride catalyzes the homocoupling of benzylic halides and benzylic gem-dibromides to give the corresponding bibenzyl and stilbenyl systems. Exposure of benzylic bromides to Ti(III) in the presence of aldehydes gave rise to the Barbier-type products. Examples of the utility of the herein described processes are included.
