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decahydro-alpha-methylnaphthalene-1-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93963-34-9

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93963-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93963-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93963-34:
(7*9)+(6*3)+(5*9)+(4*6)+(3*3)+(2*3)+(1*4)=169
169 % 10 = 9
So 93963-34-9 is a valid CAS Registry Number.

93963-34-9SDS

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 1-(1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-1-yl)ethanol

1.2 Other means of identification

Product number -
Other names EINECS 300-776-3

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:93963-34-9 SDS

93963-34-9Upstream product

93963-34-9Downstream Products

93963-34-9Relevant academic research and scientific papers

Selective catalytic hydrogenation of polycyclic aromatic hydrocarbons promoted by ruthenium nanoparticles

Bresó-Femenia, Emma,Chaudret, Bruno,Castillón, Sergio

, p. 2741 - 2751 (2015/05/27)

Ru nanoparticles stabilised by PPh3 are efficient catalysts for hydrogenation of polycyclic aromatic hydrocarbons (PAHs) containing 2-4 rings under mild reaction conditions. These compounds were partially hydrogenated with good to excellent selectivities just by optimizing the reaction conditions. The influence of the nature of substituents present in different positions of naphthalene on the selectivity of hydrogenation was also studied. Hydrogenation of products containing substituents at position 1 is slower than that of products containing substituents at position 2. In all cases, hydrogenation takes place mainly on the less substituted ring.

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