241127-72-0 Usage
Description
Benzaldehyde, 2-bromo-3,6-dihydroxy(9CI) is a chemical compound with the molecular formula C7H5BrO3. It is a derivative of benzaldehyde, a common building block in organic synthesis. The presence of the bromine and hydroxyl groups in this compound makes it useful for a variety of chemical reactions and processes, including pharmaceutical and agrochemical synthesis. It is also known for its sweet, almond-like aroma, making it a popular ingredient in the fragrance and flavoring industry.
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
Benzaldehyde, 2-bromo-3,6-dihydroxy(9CI) is used as an intermediate in the production of various chemicals for pharmaceutical and agrochemical synthesis. Its unique structure with bromine and hydroxyl groups allows for versatile chemical reactions, making it a valuable component in the synthesis of a wide range of compounds.
Used in Fragrance and Flavoring Industry:
Due to its sweet, almond-like aroma, Benzaldehyde, 2-bromo-3,6-dihydroxy(9CI) is used as a key ingredient in the fragrance and flavoring industry. Its pleasant scent and flavor profile make it suitable for use in a variety of products, including perfumes, colognes, and food products.
Used in Research and Industrial Applications:
Benzaldehyde, 2-bromo-3,6-dihydroxy(9CI) is widely used in research and industrial applications due to its versatility and unique properties. Its ability to participate in various chemical reactions and processes makes it a valuable tool for scientists and researchers in the development of new compounds and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 241127-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,1,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 241127-72:
(8*2)+(7*4)+(6*1)+(5*1)+(4*2)+(3*7)+(2*7)+(1*2)=100
100 % 10 = 0
So 241127-72-0 is a valid CAS Registry Number.
241127-72-0Relevant articles and documents
Asymmetric Total Syntheses and Structure Revisions of Eurotiumide A and Eurotiumide B, and Their Evaluation as Natural Fluorescent Probes
Nakayama, Atsushi,Sato, Hideo,Karanjit, Sangita,Hayashi, Naoki,Oda, Masataka,Namba, Kosuke
, p. 4013 - 4017 (2018)
Asymmetric total syntheses and structure revisions of dihydroisocoumarin-type natural products, eurotiumide A and eurotiumide B have been described. The key features of these total syntheses are the asymmetric Shi epoxidation, regio- and stereoselective e
Synthesis, cytotoxicity and pro-apoptosis activity of isoquinoline quinones
Ni, Hua,Xia, Chao,Zhao, Yu
, p. 2861 - 2869 (2017)
Mansouramycins are newly isolated cytotoxic isoquinoline quinones from marine organism. To find novel anticancer agents, eighteen isoquinoline quinones 7a–7r as Mansouramycins analogs were designed and synthesized. Most of these compounds displayed modera
Total synthesis of the aglycone of IB-00208
Knueppel, Daniel,Yang, Jingyue,Cheng, Bo,Mans, Douglas,Martin, Stephen F.
, p. 5741 - 5757 (2015/08/03)
Abstract A total synthesis of the aglycone of IB-00208 was accomplished in 22 steps using a newly developed approach towards polycyclic 1,4-dioxygenated xanthones from benzocyclobutenones. The generality of this entry to xanthones was initially established on several model systems before it was successfully applied to the construction of the hexacyclic core of the natural product. A new and potentially general approach towards angularly fused benzocyclobutenones using ring-closing metathesis (RCM) was also developed.