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5467-20-9

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5467-20-9 Usage

General Description

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. However, its specific uses and potential hazards or risks should be thoroughly investigated and understood before handling or working with this compound.

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 articles and documents

Computationally Aided Absolute Stereochemical Determination of Enantioenriched Amines

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

, 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.

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