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1-(bromo-naphthalen-1-yl-methyl)naphthalene is a chemical compound with the molecular formula C18H13Br. It is a derivative of naphthalene, consisting of a naphthalene core with a 1-(bromo-naphthalen-1-yl-methyl) group attached. 1-(bromo-naphthalen-1-yl-methyl)naphthalene is likely used in research or laboratory settings and may have specific applications in organic synthesis, pharmaceuticals, or materials science. As a halogenated naphthalene derivative, 1-(bromo-naphthalen-1-yl-methyl)naphthalene may have unique chemical reactivity and properties that make it useful for various purposes in the field of chemistry.

5467-20-9

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5467-20-9 Usage

Uses

Used in Organic Synthesis:
1-(bromo-naphthalen-1-yl-methyl)naphthalene is used as a building block for [the synthesis of various organic compounds] due to [its unique chemical reactivity and properties].
Used in Pharmaceutical Industry:
1-(bromo-naphthalen-1-yl-methyl)naphthalene is used as an intermediate for [the development of new pharmaceutical compounds] because of [its potential to be modified and incorporated into drug molecules].
Used in Materials Science:
1-(bromo-naphthalen-1-yl-methyl)naphthalene is used as a component in [the creation of novel materials with specific properties] for [applications such as electronics, optics, or coatings].

Check Digit Verification of cas no

The CAS Registry Mumber 5467-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5467-20:
(6*5)+(5*4)+(4*6)+(3*7)+(2*2)+(1*0)=99
99 % 10 = 9
So 5467-20-9 is a valid CAS Registry Number.

5467-20-9SDS

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 1-[bromo(naphthalen-1-yl)methyl]naphthalene

1.2 Other means of identification

Product number -
Other names bromodinaphthalen-1-ylmethane

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:5467-20-9 SDS

5467-20-9Downstream Products

5467-20-9Relevant academic research and scientific papers

Computationally Aided Absolute Stereochemical Determination of Enantioenriched Amines

Zhang, Jun,Gholami, Hadi,Ding, Xinliang,Chun, Minji,Vasileiou, Chrysoula,Nehira, Tatsuo,Borhan, Babak

supporting information, p. 1362 - 1365 (2017/03/23)

A simple and efficient protocol for sensing the absolute stereochemistry and enantiomeric excess of chiral monoamines is reported. Preparation of the sample requires a single-step reaction of the 1,1′-(bromomethylene)dinaphthalene (BDN) with the chiral amine. Analysis of the exciton coupled circular dichroism generated from the BDN-derivatized chiral amine sample, along with comparison to conformational analysis performed computationally, yields the absolute stereochemistry of the parent chiral monoamine.

Synthesis of chiral C1-symmetric N-heterocyclic carbene ligands: Application toward copper-catalyzed homocoupling of 2-naphthols

Holtz-Mulholland, Michael,Collins, Shawn K.

supporting information, p. 375 - 380 (2014/02/14)

Novel chiral C 1-symmetric NHC ligands can be prepared via dialkylation of chiral imidazoline scaffolds. Asymmetry in the ligand/metal complexes results from a chiral relay effect. The C 1-symmetric nature of the NHC ligand was proposed to allow for improved reactivity versus other achiral and chiral NHC complexes. The benefit of such ligands was demonstrated in copper-catalyzed oxidative coupling reactions. Georg Thieme Verlag KG Stuttgart · New York.

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