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25458-45-1

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25458-45-1 Usage

General Description

4-(Methoxymethoxy)bromobenzene is a chemical compound with the molecular formula C8H9BrO2. It is a derivative of bromobenzene with two methoxymethoxy (MOM) groups attached to the benzene ring. 4-(Methoxymethoxy)bromobenzene is commonly used in organic synthesis as a building block for more complex molecules. It is often utilized as a protecting group for alcohols and phenols, allowing for specific reactions to occur at other functional groups without affecting the alcohol or phenol groups. Additionally, 4-(Methoxymethoxy)bromobenzene has been studied for its potential applications in medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 25458-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25458-45:
(7*2)+(6*5)+(5*4)+(4*5)+(3*8)+(2*4)+(1*5)=121
121 % 10 = 1
So 25458-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BrO2/c1-10-6-11-8-4-2-7(9)3-5-8/h2-5H,6H2,1H3

25458-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-(methoxymethoxy)benzene

1.2 Other means of identification

Product number -
Other names p-methoxymethoxybromobenzene

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:25458-45-1 SDS

25458-45-1Relevant articles and documents

Enantioselective syntheses of (S)- and (R)-8,9 dihydroxydihydromagnolol

Gu, Wenxin,She, Xuegong,Pan, Xinfu,Yang, Teng-Kuei

, p. 1377 - 1380 (1998)

8,9-Dihydroxydihydromagnolol 5 was synthesized in four steps in which the synthesis of magnolol 4 was improved and the absolute configuration of 5 was confirmed as (R).

Chemistry-oriented synthesis (ChOS) and target deconvolution on neuroprotective effect of a novel scaffold, oxaza spiroquinone

Venkanna, Arramshetti,Cho, Kyo Hee,Dhorma, Lama Prema,Kumar, Duddukuri Nandan,Hah, Jung Mi,Park, Hyeung-geun,Kim, Sun Yeou,Kim, Mi-hyun

, p. 453 - 480 (2019)

Here we first time report an unprecedented and unnatural six-membered 1,5-oxaza spiroquinone scaffold with structural novelty, a convenient and efficient synthetic route was developed for the synthesis of new 1,5-oxaza spiroquinone derivatives (1a-1r) in

The Catalytic Asymmetric Intermolecular Prins Reaction

Diáz-Oviedo, C. David,Maji, Rajat,List, Benjamin

supporting information, p. 20598 - 20604 (2021/12/14)

Despite their significant potential, catalytic asymmetric reactions of olefins with formaldehyde are rare and metal-free approaches have not been previously disclosed. Here we describe an enantioselective intermolecular Prins reaction of styrenes and paraformaldehyde to form 1,3-dioxanes, using confined imino-imidodiphosphate (iIDP) Br?nsted acid catalysts. Isotope labeling experiments and computations suggest a concerted, highly asynchronous addition of an acid-activated formaldehyde oligomer to the olefin. The enantioenriched 1,3-dioxanes can be transformed into the corresponding optically active 1,3-diols, which are valuable synthetic building blocks.

SSAO INHIBITORS AND USES THEREOF

-

Paragraph 00488, (2020/01/08)

Described herein are compounds that are semicarbazide-sensitive amine oxidase (SSAO) inhibitors, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in treating or preventing a liver disease or condition.

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