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4456-80-8

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4456-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4456-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4456-80:
(6*4)+(5*4)+(4*5)+(3*6)+(2*8)+(1*0)=98
98 % 10 = 8
So 4456-80-8 is a valid CAS Registry Number.

4456-80-8Relevant articles and documents

COLORING RESIN COMPOSITION, COLOR FILTER, AND IMAGE DISPLAY DEVICE

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Paragraph 0211; 0214; 0215, (2018/06/06)

PROBLEM TO BE SOLVED: To provide a coloring resin composition that has high color purity, satisfies heat resistance, light resistance, and a voltage retention rate necessary for long-term reliability, which are required in the production process of a color display, and does not color migration to an adjacent color pattern. SOLUTION: A coloring resin composition contains a colorant, a solvent and a binder resin. The colorant contains a multimer of a triarylmethane-based compound having a naphthalene ring represented by dye B. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

HISTONE DEACETYLASE INHIBITORS AS THERAPEUTICS FOR NEUROLOGICAL DISEASES

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Page/Page column 50; 51, (2008/06/13)

The invention provides HDAC inhibitors that may be used as therapeutics for the treatment of a neurodegenerative or neuromuscular condition. The invention provides compounds of formula I. The invention also provides pharmaceutical compositions and articles of manufacture that include these compounds, as well as methods of treating and methods of preventing or delaying the onset of a neurodegenerative or neuromuscular condition.

Ni0-induzierte und -katalysierte Herstellung ungesaettigter Adipinsaeureanilide

Hoberg, Heinz,Baerhausen, Dieter

, p. 401 - 409 (2007/10/02)

It is shown that 4-pentencarboxylic acid anilide (I), which can readily be prepared catalytically from ethene and phenyl isocyanate (II), further reacts with II on ligand-nickel(0)-systems in a highly regioselective reaction to form triphenylphosphine-5-azanickelacyclopentan-4-one (Va).Protonolysis of Va leads to adipic acid anilide.When Va is treated with maleic acid anhydride at 20 deg C. a β'-H-elimination, is induced because the hydrolysis gives the symmetric 3-hexendicarboxylic acid dianilide (XII) with high selectivity.The catalytic reaction of I and II on a ligand-nickel(0)-complex (ligand = tricyclohexyl-phosphite) involves a β-H-elimination to yield 2-hexendicarboxylic acid dianilide (XI).This opens up the possibility of producing adipic acid derivatives catalytically in a two step synthesis from ethene and phenyl isocyanate.The mechanisms and special features are discussed.

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