Cas 360784-16-3,3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione

360784-16-3

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Basic information

Product Name: 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione
Synonyms: 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione
CAS NO:360784-16-3
Molecular Formula:
Molecular Weight: 600.369
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: 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione(360784-16-3)
EPA Substance Registry System: 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-chloro-3-cyclobutene-1,2-dione(360784-16-3)

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: 360784-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 360784-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,7,8 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 360784-16:
(8*3)+(7*6)+(6*0)+(5*7)+(4*8)+(3*4)+(2*1)+(1*6)=153
153 % 10 = 3
So 360784-16-3 is a valid CAS Registry Number.

360784-16-3Upstream product

2892-63-9 3,4-Dichlorocyclobut-3-ene-1,2-dione

360784-16-3Downstream Products

360784-17-4 3-{4-[bis(2-hexyloctyl)amino]phenyl}-4-hydroxy-3-cyclobutene-1,2-dione

360784-16-3Relevant academic research and scientific papers

Bis-, tris-, and tetrakis(squaraines) linked by stilbenoid scaffolds

Gerold, Jürgen,Holzenkamp, Uta,Meier, Herbert

, p. 2757 - 2763 (2001)

The oligosquaraines 1-5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b-15b and 17b. The target compounds exhibit in

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