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60633-91-2

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60633-91-2 Usage

Description

2-(Bromomethyl)benzaldehyde is an organic compound characterized by the presence of a bromomethyl group and a benzaldehyde moiety. It is a versatile intermediate in organic synthesis and has potential applications in various chemical and pharmaceutical processes.

Uses

Used in Chemical Synthesis:
2-(Bromomethyl)benzaldehyde is used as a key intermediate for the preparation of triiron complexes of PDK, a porphyrin-linked dicarboxylate ligand. This application is significant in the development of new materials and compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
2-(Bromomethyl)benzaldehyde can be utilized as a building block in the synthesis of pharmaceutical compounds, particularly those with potential therapeutic properties. Its unique structure allows for the creation of novel drug candidates that can target specific biological pathways or receptors.
Used in Material Science:
In the field of material science, 2-(Bromomethyl)benzaldehyde can be employed in the development of new materials with unique properties. Its ability to form complexes with metal ions, such as triiron, can lead to the creation of advanced materials with potential applications in various sectors, including electronics, energy, and environmental technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 60633-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,3 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60633-91:
(7*6)+(6*0)+(5*6)+(4*3)+(3*3)+(2*9)+(1*1)=112
112 % 10 = 2
So 60633-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO/c9-5-7-3-1-2-4-8(7)6-10/h1-4,6H,5H2

60633-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(bromomethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-(bromomethyl)

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:60633-91-2 SDS

60633-91-2Relevant articles and documents

Intracellular Generation of a Diterpene-Peptide Conjugate that Inhibits 14-3-3-Mediated Interactions

Parvatkar, Prakash,Kato, Nobuo,Uesugi, Motonari,Sato, Shin-Ichi,Ohkanda, Junko

, p. 15624 - 15627 (2015)

Synthetic agents that disrupt intracellular protein-protein interactions (PPIs) are highly desirable for elucidating signaling networks and developing new therapeutics. However, designing cell-penetrating large molecules equipped with the many functional

A Highly Fluorinated Chiral Aldehyde for Enantioselective Fluorescent Recognition in a Biphasic System

Wang, Chao,Wu, Xuedan,Pu, Lin

, p. 10749 - 10752 (2017)

A 1,1′-bi-2-naphthol (BINOL)-based aldehyde containing four perfluoroalkyl groups has been designed and synthesized. It shows enantioselective fluorescence enhancement at 420 nm when treated with the enantiomers of trans-1,2-diaminocyclohexane in an organ

Compound with PPAR delta agonistic activity, pharmaceutical composition and medical application

-

Paragraph 0061-0065, (2021/03/13)

The invention discloses a compound with PPAR delta agonistic activity, a pharmaceutical composition and medical application, wherein the structure of the compound is shown as a formula I in the specification. The compound shown in the formula I is a novel

An Intramolecular Cycloaddition Approach to the Kauranoid Family of Diterpene Metabolites

Callebaut, Brenda,Hullaert, Jan,Van Hecke, Kristof,Winne, Johan M.

supporting information, p. 310 - 314 (2019/01/10)

Synthetic studies toward the ent-kauranoid family of diterpene natural products are reported. An intramolecular (4 + 3) cycloaddition allows the direct elaboration of diverse natural product frameworks, encompassing a challenging bicyclo[3.2.1]octane core. The established routes comprise only a few synthetic operations (3-5 steps), transforming a range of simple starting materials into the tetracyclic scaffolds that are commonly found in many ent-kaurene metabolites.

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