Cas 1393090-70-4,1-(2-hydroxyphenyl(2-(4,6-dimethylpyrimidinyl)amino)methyl)naphthalene-2,7-diol

1393090-70-4

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Basic information

Product Name: 1-(2-hydroxyphenyl(2-(4,6-dimethylpyrimidinyl)amino)methyl)naphthalene-2,7-diol
Synonyms:
CAS NO:1393090-70-4
Molecular Formula:
Molecular Weight: 387.438
EINECS: N/A
Product Categories: N/A
Mol File: 1393090-70-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(2-hydroxyphenyl(2-(4,6-dimethylpyrimidinyl)amino)methyl)naphthalene-2,7-diol(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-hydroxyphenyl(2-(4,6-dimethylpyrimidinyl)amino)methyl)naphthalene-2,7-diol(1393090-70-4)
EPA Substance Registry System: 1-(2-hydroxyphenyl(2-(4,6-dimethylpyrimidinyl)amino)methyl)naphthalene-2,7-diol(1393090-70-4)

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: 1393090-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1393090-70-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,0,9 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1393090-70:
(9*1)+(8*3)+(7*9)+(6*3)+(5*0)+(4*9)+(3*0)+(2*7)+(1*0)=164
164 % 10 = 4
So 1393090-70-4 is a valid CAS Registry Number.

1393090-70-4Upstream product

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1393090-70-4Relevant articles and documents

An efficient green MCR protocol for the synthesis of new Betti bases via Mannich-type reaction

Olyaei, Abolfazl,Zarnegar, Mojgan,Sadeghpour, Mahdieh,Rezaei, Mortaza

experimental part, p. 451 - 456 (2012/09/25)

An efficient solvent and catalyst-free synthesis of new Betti base derivatives via Mannich-type one-pot threecomponent condensation reaction of aminodiazines, salicylaldehyde and naphthols under solvent-free conditions is described. The reactions occur at

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