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5,7-Dimethyl-1-naphthol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31706-76-0

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31706-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31706-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31706-76:
(7*3)+(6*1)+(5*7)+(4*0)+(3*6)+(2*7)+(1*6)=100
100 % 10 = 0
So 31706-76-0 is a valid CAS Registry Number.

31706-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dimethylnaphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 1-Naphthol,5,7-dimethyl

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:31706-76-0 SDS

31706-76-0Downstream Products

31706-76-0Relevant academic research and scientific papers

New repertoire of 'donor-two-acceptor' NIR fluorogenic dyes

Kisin-Finfer, Einat,Shabat, Doron

, p. 3602 - 3608 (2013)

Dye molecules with various fluorescent wavelengths are widely used for diagnostic and optical imaging applications. Accordingly, there is a constant demand for fluorogenic dyes with new properties. We have recently developed a novel strategy for the desig

Oxidative bromination of ketones using ammonium bromide and oxone

MacHarla, Arun Kumar,Chozhiyath Nappunni, Rohitha,Marri, Mahender Reddy,Peraka, Swamy,Nama, Narender

scheme or table, p. 191 - 195 (2012/01/17)

A highly efficient, environmentally safe and economic method for selective α-monobromination of aralkyl, cyclic, acyclic, 1,3-diketones and β-keto esters and α,α-dibromination of 1,3-diketones and β-keto esters without catalyst is reported using ammonium bromide as a bromine source and oxone as an oxidant. The reaction proceeds at ambient temperature and yields range from moderate to excellent. Bromination of unsymmetrical ketones takes place at the less substituted α-position predominantly. Aromatisation of tetralones is also carried out with this reagent system.

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