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67563-72-8

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67563-72-8 Usage

Description

1-(3-Bromopropoxy)-2-methoxybenzene is a chemical compound with the molecular formula C10H13BrO2. It is a derivative of benzene with a bromopropoxy group and a methoxy group attached at different carbon positions.
Used in Organic Synthesis:
1-(3-Bromopropoxy)-2-methoxybenzene is used as a building block for the production of various organic compounds.
Used in Medicinal Chemistry:
1-(3-Bromopropoxy)-2-methoxybenzene is used as an intermediate in the synthesis of pharmaceuticals.
Used in Agrochemicals:
1-(3-Bromopropoxy)-2-methoxybenzene is used as an intermediate in the synthesis of agrochemicals.
Used in Material Science:
1-(3-Bromopropoxy)-2-methoxybenzene may have potential applications in material science.
Used in Laboratory Research:
1-(3-Bromopropoxy)-2-methoxybenzene is used as a reagent in laboratory research.
The chemical properties and potential uses of 1-(3-Bromopropoxy)-2-methoxybenzene make it a valuable compound for various industries and scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 67563-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,6 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67563-72:
(7*6)+(6*7)+(5*5)+(4*6)+(3*3)+(2*7)+(1*2)=158
158 % 10 = 8
So 67563-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BrO2/c1-12-9-5-2-3-6-10(9)13-8-4-7-11/h2-3,5-6H,4,7-8H2,1H3

67563-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromopropoxy)-2-methoxybenzene

1.2 Other means of identification

Product number -
Other names -

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:67563-72-8 SDS

67563-72-8Relevant articles and documents

Discovery of Carboline Derivatives as Potent Antifungal Agents for the Treatment of Cryptococcal Meningitis

Tu, Jie,Li, Zhuang,Jiang, Yanjuan,Ji, Changjin,Han, Guiyan,Wang, Yan,Liu, Na,Sheng, Chunquan

, p. 2376 - 2389 (2019/03/07)

Clinical treatment of cryptococcal meningitis (CM) remains a significant challenge because of the lack of effective and safe drug therapies. Developing novel CM therapeutic agents with novel chemical scaffolds and new modes of action is of great importanc

Synthesis and pharmacological evaluation of N-acyl-1,2,3,4- tetrahydroisoquinoline derivatives as novel specific bradycardic agents

Kubota, Hideki,Watanabe, Toshihiro,Kakefuda, Akio,Masuda, Noriyuki,Wada, Kouichi,Ishii, Noe,Sakamoto, Shuichi,Tsukamoto, Shinichi

, p. 871 - 882 (2007/10/03)

A series of N-acyl-1,2,3,4-tetrahydroisoquinoline derivatives were synthesized and evaluated for their bradycardic activities in isolated guinea pig right atria and in urethane-anesthetized rats. These efforts resulted in identification of the compound 8a

Cyclotriveratrylene models for proteins: 3:1 subsite differentiation and modulation of the redox potential

Strijdonck, Gino P. F. van,Haare, John A. E. H. van,Hoenen, Paulus J.M.,Schoor, Roger C. G. M. van den,Feiters, Martinus C.,et al.

, p. 449 - 462 (2007/10/03)

The potential of cyclotriveratrylene (ctv) (2,3,7,8,12,13-hexamethoxy-10,15-dihydro-5H-tribenzocyclo-nonene) trithiols as ligands that can easily be functionalised and show subsite differentiation in their complexes with clusters has been explored.The cluster complexes of tris(2-sulfanylethoxy)- and tris(3-sulfanyl-methylbenzyloxy)-functionalised ctvs have been studied by core-extrusion experiments, spectroscopy and electrochemical techniques.With 2- as starting material a cluster complex was obtained in which the unique Fe and its co-ordinating Cl was turned into the cavity and show no reactivity.Starting with the more bulky t)4>2- the unique iron points outwards and is susceptible to substitution reactions.The effects of hydrogen bonding and electron density on the redox potential of the cluster complex have been investigated.The redox potential becomes more negative when the length of the spacer between the ctv and cluster core is increased, which is explained by the longer distance between the cluster and the electron-withdrawing phenoxy moiety of the ctv.The synthesis of ctv derivatives with one thiol and one alcohol functionality per phenyl unit, and comparison with corresponding derivatives where hydrogen bonding is not possible, showed that no significant differences were found.The effects of a substituent in an aromatic amide group that could hydrogen bond to the co-ordinated thiol were investigated.A weak effect, in the direction expected, was found upon substitution of methyl for H.

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