98015-07-7

Basic information

• Product Name: 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane
• Synonyms: 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane;1,3-Dioxolane, 2-(2-bromo-5-methoxyphenyl)-
• CAS NO: 98015-07-7
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.09654
• Product Categories: alkyl bromide
• Mol File: 98015-07-7.mol
• Article Data: 37

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane(98015-07-7)
• EPA Substance Registry System: 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane(98015-07-7)

Safety Data

• Hazardous Substances Data: 98015-07-7(Hazardous Substances Data)

Usage

Dioxolane derivative

A type of organic compound This compound is derived from a dioxolane, which is a six-membered heterocycle containing two oxygen atoms at opposite positions in the ring.

Bromine atom

A halogen atom The compound has a bromine atom attached to a phenyl ring, which can influence its chemical reactivity and properties.

Methoxy group

An organic functional group The presence of a methoxy group (-OCH3) attached to the phenyl ring contributes to the compound's unique characteristics and reactivity.

Research and pharmaceutical applications

Common uses 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane is often used in research and pharmaceutical settings for its potential applications in drug development and chemical synthesis.

Potential drug development

Possible use in new drugs The compound may have potential uses in the development of new drugs due to its unique structure and reactivity.

Chemical synthesis reagent

Use as a reagent It can also serve as a reagent in chemical synthesis, aiding in the formation of other compounds.

Controlled laboratory environment

Proper handling 2-(2-broMo-5-Methoxyphenyl)-1,3-dioxolane should be handled with care and used in a controlled laboratory environment to minimize potential hazards and toxicity risks.

Potential hazards and toxicity

Safety concerns The compound may pose potential hazards and toxic effects, so it's essential to follow proper safety protocols and precautions when working with it.

Upstream product

• 7507-86-0 2-bromo-5-methoxy-benzaldehyde 
• 107-21-1 ethylene glycol 
• 591-31-1 3-methoxy-benzaldehyde 
• 20357-24-8 5-methoxy-2-nitro-benzaldehyde 
• 26831-52-7 2-amino-5-methoxybenzaldehyde 
• 104-15-4 toluene-4-sulfonic acid 
• 150192-39-5 2-Bromo-5-methoxybenzyl alcohol 
• 22921-68-2 2-bromo-5-methoxy-benzoic acid 

Downstream Products

• 208399-40-0 3-[2-(1,3-dioxolan-2-yl)-4-methoxyphenoxy]benzaldehyde 
• 98015-08-8 2-<2-(1,3-dioxalanyl)>-4-methoxybenzaldehyde 
• 394-50-3 3-fluorosalicylaldehyde 

Relevant articles and documents

Phosphine-Catalyzed Intramolecular Vinylogous Aldol Reaction of α-Substituted Enones

We demonstrate the first phosphine-catalyzed intramolecular vinylogous aldol reaction (IVAR) of α-substituted enones. This strategy provides access to various pentannulated (hetero)arenes and dibenzocycloheptanones incorporated with two contiguous stereocenters, one of which is an all-carbon quaternary center. The scope of this work is further broadened through elaborations of the IVAR adducts to (i) benzannulated nine-membered carbocyclic systems, (ii) interesting classes of 1,3-dienes, 1,3,5-trienes, and 1-yn-3,5-dienes, and (iii) the analogs of echinolactone D and russujaponol F.

Copper-Catalyzed Tandem Cross-Coupling and Alkynylogous Aldol Reaction: Access to Chiral Exocyclic α-Allenols

An enantioselective copper-catalyzed tandem cross-coupling/alkynylogous aldol reaction has been developed. The tetrasubstituted allenoates containing both central and axial chirality have been obtained in moderate to good yields and excellent enantio-and

Chiral phosphine nitrogen phosphine ligand and chiral metal organic coordination complex and application

The invention discloses a chiral phosphine nitrogen phosphine ligand and chiral metal organic coordination complex and application. The chiral tridentate phosphine nitrogen phosphine ligand is shown as a formula (I), and the chiral metal organic coordination complex is shown as a formula (II), wherein the chiral metal organic coordination complex shown as the formula (II) is used as a homogeneouscatalyst to be applied to preparation of phenylalanine derivatives with high optical activity. The novel chiral nitrogen-phosphine ligand synthesized by taking cheap amino acid as a chiral source is applied to asymmetric hydrogenation reaction, and a chiral product with relatively high yield can be obtained with relatively low catalytic dosage, relatively short reaction time and relatively mild reaction conditions.