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15185-59-8

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15185-59-8 Usage

Description

m-Bromocinnamaldehyde, scientifically known as 3-bromocinnamaldehyde, is a chemical compound with distinctive aromatic properties. It is recognized for its sweet, pleasurable aroma and is often utilized in research and development labs, particularly in the fields of organic and medicinal chemistry. As an essential precursor in the synthesis of various compounds, m-Bromocinnamaldehyde plays a significant role in chemical research. Its molecular formula is C9H7BrO, and its bromine component makes it a valuable tool for halogenation reactions in organic synthesis. It is typically stored in a cool, ventilated area, away from ignition sources, heat, and light.

Uses

Used in Organic Chemistry Research:
m-Bromocinnamaldehyde is used as a precursor in the synthesis of various organic compounds, contributing to the development of new chemical entities and materials. Its bromine atom facilitates halogenation reactions, making it a versatile building block in organic synthesis.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, m-Bromocinnamaldehyde is employed as a starting material for the synthesis of pharmaceutical compounds. Its unique structure and reactivity enable the creation of potential drug candidates, with the aim of developing new therapeutic agents.
Used in Chemical Synthesis:
m-Bromocinnamaldehyde is used as a reagent in various chemical synthesis processes, allowing for the formation of complex molecules and structures. Its presence in these reactions can lead to the production of novel compounds with potential applications in various industries.
Used in Material Science:
m-Bromocinnamaldehyde is utilized in the development of new materials, such as polymers and composites, due to its ability to participate in various chemical reactions. Its incorporation into these materials can result in improved properties, such as enhanced stability or increased functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 15185-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15185-59:
(7*1)+(6*5)+(5*1)+(4*8)+(3*5)+(2*5)+(1*9)=108
108 % 10 = 8
So 15185-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrO/c10-9-5-1-3-8(7-9)4-2-6-11/h1-7H/b4-2+

15185-59-8SDS

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 3-(3-Bromophenyl)acrylaldehyde

1.2 Other means of identification

Product number -
Other names m-Bromzimtaldehyd

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:15185-59-8 SDS

15185-59-8Relevant articles and documents

Method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and diphosphine ligand used in method

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Paragraph 0146-0148, (2021/05/29)

The invention discloses a method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and a diphosphine ligand used in the method. According to the invention, indole-substituted phosphoramidite diphosphine ligand which is stable in air and insensitive to light is synthesized by utilizing a continuous one-pot method, and the indole-substituted phosphoramidite diphosphine ligand and a rhodium catalyst are used for jointly catalyzing to successfully achieve a hydroformylation reaction of aromatic terminal alkyne and terminal conjugated eneyne under the condition of synthesis gas for the first time, so that an olefine aldehyde structure compound can be rapidly and massively prepared, and particularly, a polyolefine aldehyde structure compound which is more difficult to synthesize in the prior art can be easily prepared and synthesized, and a novel method is provided for synthesis and modification of drug molecules, intermediates and chemical products.

Highly Enantioselective Synthesis of Functionalized Glutarimide Using Oxidative N-Heterocyclic Carbene Catalysis: A Formal Synthesis of (?)-Paroxetine

Porey, Arka,Santra, Surojit,Guin, Joyram

, p. 5313 - 5327 (2019/04/16)

A simple yet highly effective approach toward enantioselective synthesis of trans-3,4-disubstituted glutarimides from readily available starting materials is developed using oxidative N-heterocyclic carbene catalysis. The catalytic reaction involves a formal [3 + 3] annulation between enals and substituted malonamides enabling the production of glutarimide derivatives in a single chemical operation via concomitant formation of C-C and C-N bonds. The reaction offers easy access to a broad range of functionalized glutarimides with excellent enantioselectivity and good yield. Synthetic application of the method is demonstrated via formal synthesis of (?)-paroxetine and other bioactive molecules.

Secondary amine-catalyzed [3 + 3] benzannulation to access polysubstituted benzenes through iminium activation

Jiang, Lin,Li, Hang,Zhou, Jiang-Feng,Yuan, Ming-Wei,Li, Hong-Li,Chuan, Yong-Ming,Yuan, Ming-Long

supporting information, p. 336 - 343 (2018/02/09)

An organocatalytic [3 + 3] benzannulation to access polysubstituted benzenes from readily available α,β-unsaturated aldehydes and 1,3-bis(phenylsulfonyl)propene or 4-sulfonylcrotonates is described. The key reaction step is considered to be the iminium ac

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