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6-Bromo-1-methoxynaphthalene is a chemical compound that belongs to the class of organic compounds known as bromonaphthalenes. This category is comprised of compounds containing a naphthalene ring where one or more carbon atoms are substituted by a bromine atom. This specific compound gets its name from the presence of a bromine atom attached at the 6th position and a methoxyl group attached at the 1st position on the naphthalene ring. It's predominantly used in scientific research, primarily in chemistry laboratories, for its unique reactivity and other chemical properties. The exact physical properties such as melting and boiling point may vary depending on its specific arrangement and other conditions. Its molecular formula is C11H9BrO.

54828-63-6

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54828-63-6 Usage

Uses

Used in Scientific Research:
6-Bromo-1-methoxynaphthalene is used as a research chemical for its unique reactivity and chemical properties. It is particularly valuable in chemistry laboratories where its properties can be studied and utilized in various chemical reactions and processes.
Used in Chemistry Laboratories:
6-Bromo-1-methoxynaphthalene is used as a reagent in chemistry laboratories, where its specific chemical properties can be harnessed for various experimental purposes. Its reactivity with other compounds and its stability under certain conditions make it a useful tool in the synthesis of other organic compounds and in the investigation of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 54828-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,2 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54828-63:
(7*5)+(6*4)+(5*8)+(4*2)+(3*8)+(2*6)+(1*3)=146
146 % 10 = 6
So 54828-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrO/c1-13-11-4-2-3-8-7-9(12)5-6-10(8)11/h2-7H,1H3

54828-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-1-methoxynaphthalene

1.2 Other means of identification

Product number -
Other names 6-methoxy-2-bromonaphthalene

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:54828-63-6 SDS

54828-63-6Downstream Products

54828-63-6Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

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Paragraph 0152; 0153, (2019/04/08)

A compound comprising a first ligand LA having a Formula selected from: is disclosed. In the Formulas rings B and C are 5-membered or 6-membered aromatic or heteroaromatic ring; Z1, Z2, X1, X2, X3, X4, X5, and X6 are each C or N, but X1, X2, X3, or X4 is C when it forms a direct bond to Z2; Y is selected from CRR′, NR′, O, S, and Se; R, R′, RA, RB, RC, and RD are each selected from a variety of substituents; the ligand LA is coordinated to a metal M by the dashed lines, and optionally to other ligands. Organic light emitting devices and consumer products containing the compounds are also disclosed.

PHOSPHORORGANISCHE VERBINDUNGEN 108. DIE SYNTHESE FLUORESZIERENDER UND CHEMOSELEKTIVER REAGENTIEN ZUM GEZIELTEN NACHWEIS UND SCHUTZ BIOLOGISCH WICHTIGER FUNKTIONELLER GRUPPEN

Horner, Leopold,Flemming, Hans-Wolfram

, p. 345 - 362 (2007/10/02)

Compounds of type A are fluorescent, if the donator groups, like NMe2, OMe, SMe and PR2, and the acceptor groups, like R'P(O)X, SO2R' and CO2R', are linked to different nuclei of the naphthalin ring system.The chemoselectivity of the electrophilic phosphoryl compounds P(O)X to nucleophiles like ROH, RNHR' and RSH is determined by the nature of the leaving group X responsible for different reaction mechanism.Phosphoryl groups with X = Cl attack predominantly R-NHR'- groups; phosphoryl compounds with X = F and OC6H4NO2(p) are ROH-selective.In this publication compounds of type A are presented, in which fluorescence and chemoselectivity are combined by structure in one molecule.These compounds are important analytic reagents (prove of the functional groups in the active site of enzymes) and as protective groups in the synthesis of natural products like peptides.

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