5467-20-9 Usage
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.
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.
5467-20-9Relevant 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.