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162535-05-9

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162535-05-9 Usage

General Description

The chemical compound, "(4E)-4-[(4-hydroxynaphthalen-1-yl)-phenyl-methylidene]naphthalen-1-one", is a complex organic compound with a long and specific structure. It consists of a naphthalene ring with a phenyl-methylidene group attached, as well as a hydroxynaphthalen-1-yl group. (4E)-4-[(4-hydroxynaphthalen-1-yl)-phenyl-methylidene]naphthalen-1-one may have potential applications in the field of organic chemistry and may be used as a building block for the synthesis of other organic compounds. Its specific properties and potential uses would need to be further investigated through experimentation and research.

Check Digit Verification of cas no

The CAS Registry Mumber 162535-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 162535-05:
(8*1)+(7*6)+(6*2)+(5*5)+(4*3)+(3*5)+(2*0)+(1*5)=119
119 % 10 = 9
So 162535-05-9 is a valid CAS Registry Number.

162535-05-9Relevant articles and documents

Phenol-naphthol-benzeine - Synthesis and chromophoric properties. Part 5: Benzeines

Kallmayer,Lenze

, p. 534 - 536 (2007/10/03)

Phenols 4 and 1-naphthol (5) react with benzotrichloride (6) to give benzaurines 7, phenol-naphthol-benzeines 3 and α-naphtholbenzein (1), which were isolated by chromatography. Phenol-naphthol-benzeines 3 are X-/Y-chromophores like α-naphtholbenzeine (1) with two absorption maxima. These are hypsochromically shifted in neutral, in alkaline and in acidic solution, compared with those of 1.

4-[(4-hydroxy-1-naphthyl)phenylmethylen]-1(4H)-naphthalinone - The indicator substance from 'α-naphtholbenzein', part 1: Benzeines

Lenze,Kallmayer

, p. 36 - 38 (2007/10/02)

The red brown mixture of E/Z-isomeres 3/6 were isolated from 'α-naphtholbenzein', a mixture of various substances. Compounds 3 and 6 are the real indicator substances in 'α-naphtholbenzein', which is used to indicate titrations of weak bases and acids. The reduction of 3/6 give only the colorless 9. Its 4,4'-connections are proved by 1H-NMR-spectroscopy after OH-methylation.

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