71295-21-1 Usage
Description
5-Bromo-2,3-dimethoxybenzaldehyde, also known as 5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97, is an organic compound derived from the starting reagent 5-bromo-2-hydroxy-3-methoxybenzaldehyde. It is characterized by the presence of a bromine atom at the 5th position, and methoxy groups at the 2nd and 3rd positions of the benzene ring. 5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 has potential applications in various industries due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Industry:
5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific receptors or enzymes in the body.
Used in Chemical Synthesis:
In the field of organic chemistry, 5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 serves as a valuable building block for the synthesis of more complex molecules. Its bromine atom and methoxy groups can be further modified or used as starting points for the creation of a wide range of organic compounds, including dyes, pigments, and other specialty chemicals.
Used in Material Science:
The unique properties of 5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 make it a candidate for use in the development of new materials with specific characteristics. For example, its electronic and optical properties could be exploited in the creation of advanced materials for use in electronics, sensors, or other high-tech applications.
Used in Research and Development:
Due to its unique structure and potential applications, 5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 is an important compound for research and development in various scientific fields. It can be used as a model compound to study the effects of structural modifications on the properties and reactivity of organic molecules, as well as to explore new synthetic routes and methodologies.
Used in Analytical Chemistry:
5-BROMO-2 3-DIMETHOXYBENZALDEHYDE 97 can also be employed as a reference compound or standard in analytical chemistry. Its distinct chemical properties make it useful for calibrating instruments, validating analytical methods, or as a benchmark for comparing the performance of different analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 71295-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,9 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71295-21:
(7*7)+(6*1)+(5*2)+(4*9)+(3*5)+(2*2)+(1*1)=121
121 % 10 = 1
So 71295-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO3/c1-12-8-4-7(10)3-6(5-11)9(8)13-2/h3-5H,1-2H3
71295-21-1Relevant articles and documents
Synthesis method 5 - halogeno-veratraldehyde
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, (2021/11/21)
The invention belongs to the field of organic chemistry, and in particular relates 5 - to a method for synthesizing halogenated O-veratraldehyde by using 4 - halogenoylguaiacol as a raw material to obtain 2 -hydroxy -3 - methoxy -5 -halogenated mandelic a
Synthesis of N-benzyl-des-D-ring lamellarin K via an acyl-Claisen/Paal-Knorr approach
Dittrich, Nora,Pilkington, Lisa I.,Leung, Euphemia,Barker, David
, p. 1881 - 1894 (2017/03/11)
Lamellarin K is a complex pyrrole natural product and member of the lamellarin family – a group of natural products known for their potent biological activities, such as, antiproliferative activity and inhibition of P-gp mediated drug efflux pumps. We herein describe the synthesis of the N-benzyl-des-D ring analogue of lamellarin K using a route that centres on an acyl-Claisen reaction to eventually prepare a highly-functionalised 1-aryl-4-methyl-1,4-diketone. Paal-Knorr pyrrole formation using this diketone undergoes auto-oxidation to give a fully-substituted 5-formyl pyrrole which was converted into the natural lactone B ring. Antiproliferative testing of the N-benzyl-des-D ring analogue gave an IC50 of 2.63?μM against the MDA-MB-231 breast cancer cell line.
Metal triflate-catalyzed cyclization of arylvinylcarbinols: Formal synthesis of (±)-dichroanone and (±)-taiwaniaquinone H
Kakde, Badrinath N.,De, Subhadip,Dey, Dhananjay,Bisai, Alakesh
, p. 8176 - 8179 (2013/09/02)
A formal synthesis of diterpenoids viz. the taiwaniaquinoids (±)-dichroanone (1a) and (±)-taiwaniaquinone H (1b) possessing an all carbon quaternary stereocenter has been reported. The key step involves a metal triflate-catalyzed cyclization of arylvinylc
