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1-Naphthalenol, 2-[1-(phenylimino)ethyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138946-36-8

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138946-36-8 Usage

Chemical class

Naphthols (organic compounds)

Appearance

Yellowish brown solid at room temperature

Odor

Specific odor

Primary use

Raw material in the production of dyes, pigments, and pharmaceuticals

Secondary uses

Synthesis of complex organic molecules, building block for functionalization of organic compounds, manufacturing of plastics, and intermediate in various chemical processes

Safety precautions

Handle with care to avoid health and safety hazards

Check Digit Verification of cas no

The CAS Registry Mumber 138946-36-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,4 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138946-36:
(8*1)+(7*3)+(6*8)+(5*9)+(4*4)+(3*6)+(2*3)+(1*6)=168
168 % 10 = 8
So 138946-36-8 is a valid CAS Registry Number.

138946-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<15N-Phenylacetimidoyl>-<1>-naphthol

1.2 Other means of identification

Product number -
Other names 2-{1-[(E)-Phenylimino]-ethyl}-naphthalen-1-ol

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:138946-36-8 SDS

138946-36-8Downstream Products

138946-36-8Relevant academic research and scientific papers

Structural and aromatic aspects of tautomeric equilibrium in hydroxy aryl Schiff bases

Filarowski,Kochel,Kluba,Kamounah

, p. 939 - 944 (2008)

The synthesis and X-ray measurements of four Schiff bases were carried out at 100K. The HOMA and HOSE aromaticity indices wer estimated on the basis of the experimental data. The aromaticity of the phenyl ring and the chelate chain was analysed. A comparison of the aromaticity of naphthalene and phenyl derivatives of hydroxy aryl Schiff bases is presented. The balance between the aromaticity of adjacent rings of the naphthalene fragment and its effect on proton transfer is defined. Research on the interrelations between aromaticity and the intramolecular proton transfer in hydroxy aryl Schiff bases is shown. Copyright

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