Cas 93486-92-1,1,4-Naphthalenedione, 2-[1-chloro-2-(methylphenylamino)ethyl]-3-phenyl-

93486-92-1

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Basic information

Product Name: 1,4-Naphthalenedione, 2-[1-chloro-2-(methylphenylamino)ethyl]-3-phenyl-
Synonyms:
CAS NO:93486-92-1
Molecular Formula: C25H20ClNO2
Molecular Weight: 401.892
EINECS: N/A
Product Categories: N/A

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: 1,4-Naphthalenedione, 2-[1-chloro-2-(methylphenylamino)ethyl]-3-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-Naphthalenedione, 2-[1-chloro-2-(methylphenylamino)ethyl]-3-phenyl-(93486-92-1)
EPA Substance Registry System: 1,4-Naphthalenedione, 2-[1-chloro-2-(methylphenylamino)ethyl]-3-phenyl-(93486-92-1)

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: 93486-92-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93486-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93486-92:
(7*9)+(6*3)+(5*4)+(4*8)+(3*6)+(2*9)+(1*2)=171
171 % 10 = 1
So 93486-92-1 is a valid CAS Registry Number.

93486-92-1Upstream product

87537-32-4 2-phenyl-3-<1-hydroxy-2-(N-methylanilino)ethyl>-1,4-naphthoquinone

93486-92-1Downstream Products

93486-92-1Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF COMPLEXES AND AUTOCOMPLEXES WITH CHARGE TRANSFER. XLV. INTRAMOLECULAR DONOR-ACCEPTOR COMPLEXES OF THE 2-PHENYL-1,4-NAPHTHOQUINONE SERIES

Larinya, L. Ya.,Lokmane, E. Ya.,Freimanis, Ya. F.

, p. 1748 - 1752 (2007/10/02)

2-Phenyl-3--1,4-naphthoquinones, which are new intramolecular donor-acceptor complexes with a three-membered bridge, were obtained.The basicity of the donor fragments in the synthesized autocomplexes was studied, and a

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