Cas 5426-22-2,4-[(2-methoxynaphthalen-1-yl)methyl]-N,N-dimethylaniline

5426-22-2

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Basic information

Product Name: 4-[(2-methoxynaphthalen-1-yl)methyl]-N,N-dimethylaniline
Synonyms: 4-[(2-Methoxy-1-naphthyl)methyl]-N,N-dimethylaniline; benzenamine, 4-[(2-methoxy-1-naphthalenyl)methyl]-N,N-dimethyl-
CAS NO:5426-22-2
Molecular Formula: C₂₀H₂₁NO
Molecular Weight: 291.3868
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 445.2°C at 760 mmHg
Flash Point: 130.1°C
Appearance: N/A
Density: 1.099g/cm³
Vapor Pressure: 4.04E-08mmHg at 25°C
Refractive Index: 1.631
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-[(2-methoxynaphthalen-1-yl)methyl]-N,N-dimethylaniline(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(2-methoxynaphthalen-1-yl)methyl]-N,N-dimethylaniline(5426-22-2)
EPA Substance Registry System: 4-[(2-methoxynaphthalen-1-yl)methyl]-N,N-dimethylaniline(5426-22-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 5426-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 5426-22-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5426-22:
(6*5)+(5*4)+(4*2)+(3*6)+(2*2)+(1*2)=82
82 % 10 = 2
So 5426-22-2 is a valid CAS Registry Number.

5426-22-2Upstream product

5426-22-2Downstream Products

5426-22-2Relevant academic research and scientific papers

N-benzotriazoles: Preparation and Use in Synthesis

Katritzky, Alan R.,Lan, Xiangfu,Lam, Jamshed N.

, p. 1819 - 1826 (2007/10/02)

Methoxybenzenes and -naphthalenes are benzotriazolylmethylated in the para-position or if this is blocked in an ortho-position.The methylene groups in the products are readily substituted by electrophiles via the lithiated derivatives.Displacement ot the benzotriazole group can be effected by organometallic reagents or by electron-rich benzoid compounds to afford a versatile method for the synthesis of substituted aryl ethers.Key Words: Lithiation/ Grignard reaction/ Condensation/ Aryl ethers/ Diarylmethanes

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