Cas 109735-64-0,p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine

109735-64-0

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Product Name: p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine
Synonyms: p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine
CAS NO:109735-64-0
Molecular Formula:
Molecular Weight: 612.822
EINECS: N/A
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Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
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Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine(CAS DataBase Reference)
NIST Chemistry Reference: p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine(109735-64-0)
EPA Substance Registry System: p-Tolyl-{2-[2-[4-p-tolylamino-5-[(E)-p-tolylimino]-5H-thiazol-(2E)-ylidene]-eth-(E)-ylidene]-5-[(E)-p-tolylimino]-2,5-dihydro-thiazol-4-yl}-amine(109735-64-0)

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HazardClass: N/A
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Hazardous Substances Data: 109735-64-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109735-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,3 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109735-64:
(8*1)+(7*0)+(6*9)+(5*7)+(4*3)+(3*5)+(2*6)+(1*4)=140
140 % 10 = 0
So 109735-64-0 is a valid CAS Registry Number.

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109735-64-0Relevant academic research and scientific papers

MO-LCAO Calculations on Sulfur-containing ?-Electron Systems. XLIX. Tetramethine Bridged Derivatives of the Oxalic Acid - Novel Coloured Pigments of Indigoid Structure

Beckert, R.,Fabian, J.

, p. 805 - 811 (2007/10/02)

Whereas thioamides react with the oxalylchloride to Δ2-thiazoline-4,5-diones 1, which are precursors of the versatile thioacylisocyanate 2 synthons, the analogous reaction between thioamides and oxalyl-bis(arylimidchlorides) completely fails.In

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