Cas 486396-30-9,Benzoic acid, 4-[[[2-[4,5-bis(hexylthio)-1,3-dithiol-2-ylidene]-5-(methylthio)-1,3-dithiol- 4-yl]thio]methyl]-

486396-30-9

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Basic information

Product Name: Benzoic acid, 4-[[[2-[4,5-bis(hexylthio)-1,3-dithiol-2-ylidene]-5-(methylthio)-1,3-dithiol- 4-yl]thio]methyl]-
Synonyms:
CAS NO:486396-30-9
Molecular Formula: C27H36O2S8
Molecular Weight: 649.11
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: Benzoic acid, 4-[[[2-[4,5-bis(hexylthio)-1,3-dithiol-2-ylidene]-5-(methylthio)-1,3-dithiol- 4-yl]thio]methyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 4-[[[2-[4,5-bis(hexylthio)-1,3-dithiol-2-ylidene]-5-(methylthio)-1,3-dithiol- 4-yl]thio]methyl]-(486396-30-9)
EPA Substance Registry System: Benzoic acid, 4-[[[2-[4,5-bis(hexylthio)-1,3-dithiol-2-ylidene]-5-(methylthio)-1,3-dithiol- 4-yl]thio]methyl]-(486396-30-9)

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: 486396-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 486396-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,3,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 486396-30:
(8*4)+(7*8)+(6*6)+(5*3)+(4*9)+(3*6)+(2*3)+(1*0)=199
199 % 10 = 9
So 486396-30-9 is a valid CAS Registry Number.

486396-30-9Upstream product

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486396-30-9Relevant academic research and scientific papers

Synthesis of novel phthalocyanine-tetrathiafulvalene hybrids; Intramolecular fluorescence quenching related to molecular geometry

Farren, Christopher,Christensen, Christian A.,FitzGerald, Simon,Bryce, Martin R.,Beeby, Andrew

, p. 9130 - 9139 (2007/10/03)

A number of silicon phthalocyanine bis-esters have been synthesized and characterized, with axial ligands containing one or more tetrathiafulvalene groups. Variations in the substitution positions around a central aromatic "hinge" within the ligands lead

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