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33816-51-2

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33816-51-2 Usage

General Description

5-Bromo-2-methoxycyclohepta-2,4,6-trien-1-one is a chemical compound with the molecular formula C8H9BrO2. It is a substituted cycloheptatrienone with a bromine atom at the 5-position and a methoxy group at the 2-position. 5-BROMO-2-METHOXYCYCLOHEPTA-2,4,6-TRIEN-1-ONE is used in organic synthesis and as a building block for the preparation of various pharmaceuticals and agrochemicals. It may also have potential applications in the field of medicinal chemistry due to its unique structure and reactivity. Additionally, it has been studied for its potential biological activities and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 33816-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,8,1 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33816-51:
(7*3)+(6*3)+(5*8)+(4*1)+(3*6)+(2*5)+(1*1)=112
112 % 10 = 2
So 33816-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO2/c1-11-8-5-3-6(9)2-4-7(8)10/h2-5H,1H3

33816-51-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BROMO-2-METHOXYCYCLOHEPTA-2,4,6-TRIEN-1-ONE

1.2 Other means of identification

Product number -
Other names 2,4,6-Cycloheptatrien-1-one,5-bromo-2-methoxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33816-51-2 SDS

33816-51-2Relevant articles and documents

TROPOLONE DERIVATIVES AND TAUTOMERS THEREOF FOR IRON REGULATION IN ANIMALS

-

Page/Page column 197; 198, (2021/04/23)

Disclosed are a series of compounds or their tautomers having a general structure represented by Formula (la), (lb), (Ila), (lIb), or (lIc) and pharmaceutically acceptable salts thereof. The present disclosure also relates to pharmaceutical compositions comprising said compounds or tautomers. The present disclosure further relates to a method of treating a disease or condition associated with iron dysregulation or dysfunctional iron homeostasis comprising administering to a subject in need thereof a therapeutically effective amount of Formula (la), (lb), (Ila), (lIb), or (lIc) compounds or tautomers.

Efforts directed toward the synthesis of colchicine: Application of palladium-catalyzed siloxane cross-coupling methodology

Seganish, W. Michael,Handy, Christopher J.,DeShong, Philip

, p. 8948 - 8955 (2007/10/03)

Colchicine is an important and synthetically challenging natural product. The key synthetic step in this approach to the synthesis of colchicine involved a palladium-catalyzed cross-coupling reaction between 5-bromotropolone (4) and an aryl siloxane to form the aryl-tropolone bond. The coupling of a variety of highly functionalized aryl siloxane derivatives was investigated and optimized coupling conditions were developed. It was discovered that a palladium catalyst with a high degree of phosphine ligand coordination (5 equiv of phosphine/mol Pd) was necessary to efficiently couple aryl siloxanes with 5-bromotropolone (4). In addition, the coupling approach has provided a direct comparison between siloxane and boronic acid coupling technologies that demonstrated that aryl siloxanes and boronic acids produce similar yields of highly functionalized biaryl products.

Syntheses and ipso-substitution reactions of some C-stannylated troponoids

Banwell, Martin G.,Cameron, Jennifer M.,Collis, Maree P.,Gravatt, G. Lance

, p. 395 - 407 (2007/10/03)

The C-stannylated troponoids (2)-(8) have been prepared and two of these shown to undergo palladium(0)-catalysed cross-coupling with bromobenzene to give the corresponding phenyl-substituted tropone. Compounds (3), (5) and (6)-(8) all react with electrophiles to give products of ipso-substitution.

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