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Phenol, 4-(1-naphthalenylamino)-, also known as 4-(1-naphthyl)phenol or 4-aminonaphthalene-1-ol, is an organic compound with the chemical formula C15H13NO. It is a derivative of phenol, where a naphthalene ring is attached to the para position of the phenol molecule. Phenol, 4-(1-naphthalenylamino)- is a white to pale yellow crystalline solid with a melting point of approximately 90-92°C. It is used as an intermediate in the synthesis of various dyes, pharmaceuticals, and other chemical products. Due to its aromatic nature, it exhibits low solubility in water but is soluble in organic solvents such as ethanol, acetone, and benzene. The compound may have potential applications in the fields of organic synthesis, material science, and medicinal chemistry.

5924-21-0

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5924-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5924-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5924-21:
(6*5)+(5*9)+(4*2)+(3*4)+(2*2)+(1*1)=100
100 % 10 = 0
So 5924-21-0 is a valid CAS Registry Number.

5924-21-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name p-hydroxyphenyl-α-naphthylamine

1.2 Other means of identification

Product number -
Other names (4-Oxy-phenyl)-α-naphthylamin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5924-21-0 SDS

5924-21-0Relevant academic research and scientific papers

RESEARCH IN THE CHEMISTRY OF HETEROCYCLIC QUINONE IMINES. 11. EFFECT OF BENZANNELATION ON THE OXIDATIVE CYCLIZATION OF DIARYLAMINO-N-ARYL-1,4-BENZOQUINONE MONOIMINES TO PHENAZINONE DERIVATIVES

Afanas'eva, G. B.,Tsoi, E. V.

, p. 616 - 620 (2007/10/02)

2,5-Diarylamino-N-α(β)-naphthyl-1,4-benzoquinone monoimines undergo oxidative cyclization to give benzannelated phenazinone derivatives.The effect of an N-aryl fragment on the ease of cyclization decreases in the order N-β-naphthyl > N-α-naphthyl > N-phenyl. 2-Arylamino-N-phenyl-1,4-naphthoquinone monoimines do not undergo oxidative cyclization to phenazinones.

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