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60633-78-5

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60633-78-5 Usage

General Description

2-(2-Bromoethoxy)benzenecarbaldehyde is a chemical compound with the molecular formula C9H9BrO2. It is a benzaldehyde derivative that contains a bromoethoxy group on the benzene ring. 2-(2-BROMOETHOXY)BENZENECARBALDEHYDE is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It can also be used as a reagent in the synthesis of various organic compounds. 2-(2-Bromoethoxy)benzenecarbaldehyde is a colorless to pale yellow liquid with a strong aromatic odor, and it is considered to be potentially hazardous if not handled and used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 60633-78-5 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, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60633-78:
(7*6)+(6*0)+(5*6)+(4*3)+(3*3)+(2*7)+(1*8)=115
115 % 10 = 5
So 60633-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO2/c10-5-6-12-9-4-2-1-3-8(9)7-11/h1-4,7H,5-6H2

60633-78-5SDS

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-(2-Bromoethoxy)Benzaldehyde

1.2 Other means of identification

Product number -
Other names 2-(2-bromoethoxy)benzaldehyde

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:60633-78-5 SDS

60633-78-5Relevant articles and documents

Selective detection of Hg(II) with benzothiazole-based fluorescent organic cation and the resultant complex as a ratiometric sensor for bromide in water

Singh, Amanpreet,Singh, Ajnesh,Singh, Narinder,Jang, Doo Ok

, p. 3535 - 3541 (2016)

A benzothiazole-based receptor conjugated with an imidazolium cation, receptor N1, was synthesized. Receptor N1 is capable of selectively binding Hg(II) in the presence of other metal ions in water, with a large enhancement in fluorescence intensity at 38

Design, synthesis, in silico and in vitro studies for new nitric oxide‐releasing indomethacin derivatives with 1,3,4‐oxadiazole‐2‐thiol scaffold

Sava, Alexandru,Buron, Frederic,Routier, Sylvain,Panainte, Alina,Bibire, Nela,Constantin, Sandra M?d?lina,Lupa?cu, Florentina Geanina,Foc?a, Alin Viorel,Profire, Lenu?a

, (2021/07/07)

Starting from indomethacin (IND), one of the most prescribed non‐steroidal anti‐inflammatory drugs (NSAIDs), new nitric oxide‐releasing indomethacin derivatives with 1,3,4‐oxadiazole‐ 2‐thiol scaffold (NO‐IND‐OXDs, 8a‐p) have been developed as a safer and

Iron-catalyzed protodehalogenation of alkyl and aryl halides using hydrosilanes

Pilli, Ramadevi,Balakrishnan, Venkadesh,Chandrasekaran, Revathi,Rasappan, Ramesh

supporting information, p. 1749 - 1753 (2019/02/20)

A simple and efficient iron-catalyzed protodehalogenation of alkyl and aryl halides using phenylhydrosilane is disclosed. The reaction utilizes FeCl3 without the requirement of ligands. Unactivated alkyl and aryl halides were successfully reduced in good yields; sterically hindered tertiary halides were also reduced including the less reactive chlorides. The scalability of this methodology was demonstrated by a gram-scale synthesis with a catalyst loading as low as 0.5 mol%. Notably, disproportionation of phenylsilane leads to diphenylsilane that further reduces the halides. Preliminary mechanistic studies revealed a non-radical pathway and the source of hydrogen is PhSiH3via deuterium labeling studies. Our methodology represents simplicity and provides a good alternative to typical tin, aluminum and boron hydride reagents.

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