90109-64-1 Usage
Description
3-Bromo-4,5-diethoxy-benzaldehyde is a chemical compound characterized by the molecular formula C11H13BrO3. It is a pale yellow solid with a molecular weight of 269.12 g/mol. 3-BROMO-4,5-DIETHOXY-BENZALDEHYDE is utilized in various fields due to its unique properties and potential applications.
Uses
Used in Organic Synthesis:
3-Bromo-4,5-diethoxy-benzaldehyde is employed as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure allows it to be a versatile component in creating a wide range of products.
Used in Chemical Research and Development:
3-BROMO-4,5-DIETHOXY-BENZALDEHYDE also serves as a reagent in chemical research and development, where it aids in the advancement of new chemical processes and the discovery of novel substances.
Used in Materials Science:
3-Bromo-4,5-diethoxy-benzaldehyde has potential applications in the field of materials science. It is being studied for its properties as a functional material in the production of sensors and organic electronic devices, which could contribute to the development of innovative technologies.
Safety Precautions:
It is important to handle 3-Bromo-4,5-diethoxy-benzaldehyde with caution, as it is a hazardous material. Contact with skin and eyes can cause irritation, so proper safety measures should be taken during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 90109-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90109-64:
(7*9)+(6*0)+(5*1)+(4*0)+(3*9)+(2*6)+(1*4)=111
111 % 10 = 1
So 90109-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13BrO3/c1-3-14-10-6-8(7-13)5-9(12)11(10)15-4-2/h5-7H,3-4H2,1-2H3
90109-64-1Relevant articles and documents
Sulfur Analogues of Psychotomimetic Agents. 3. Ethyl Homologues of Mescaline and Their Monothio Analogues
Jacob, Peyton,Shulgin, Alexander T.
, p. 881 - 888 (2007/10/02)
All possible monothio analogues of the mono-, di-, and triethoxy homologues of mescaline have been synthesized and pharmacologically evaluated in man.Modifications at the ring position para to the ethylamine chain, either with a sulfur atom, a longer alkyl chain, or both, lead to compounds of high central nervous system activity.The 4-n-propoxy and 4-n-butoxy homologues and their corresponding 4-thio analogues were also synthesized and pharmacologically evaluated.The propyl homologues retain high potency, but a butyl group (either with or without a sulfur atom) leads to a decrease in activity.The m-ethyl or m-thio analogues retain some central action but the diethoxy and especially the triethoxy homologues are relatively inactive as psychotomimetic drugs.