Welcome to LookChem.com Sign In|Join Free
  • or
dimethyl naphthalene-1,2-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10060-32-9

Post Buying Request

10060-32-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

10060-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10060-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,6 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10060-32:
(7*1)+(6*0)+(5*0)+(4*6)+(3*0)+(2*3)+(1*2)=39
39 % 10 = 9
So 10060-32-9 is a valid CAS Registry Number.

10060-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl naphthalene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 1,2-naphthalenedicarboxylate

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:10060-32-9 SDS

10060-32-9Downstream Products

10060-32-9Relevant academic research and scientific papers

MOFs come up to scratch: An environmentally benign route to oxidative [4 + 2] cycloaddition on maleimides solely: Via MOFs in water

Abbasnia, Masoumeh,Bahmani, Mona,Sheykhan, Mehdi,Taghizadeh, Parvaneh

, p. 3216 - 3228 (2020)

The first Diels-Alder reaction of vinyl arenes with ene systems catalyzed by MOFs is reported. Maleimides and maleic anhydride were annulated/dehydrogenated on styrenes in the presence of a mixed-metal (FeNi)MIL-88A catalyst. Neither an additional oxidant nor a source of halogen is needed to drive this oxidative [4 + 2] cyclization reaction. Kinetic evidence such as activation entropy corroborates the proposed concerted mechanism. The reaction proceeds merely through a cost-effective catalyst in water as the greenest solvent. The product of annulation of styrene with maleic anhydride was used for the first L-selective annulative π-extension on naphthalene.

Method for purifying a crude dimethyl naphthalene dicarboxylate

-

, (2008/06/13)

A method for purifying a dimethyl naphthalene dicarboxylate produced from a naphthalene dicarboxylic acid which is in turn produced by the liquid phase oxidation of a dialkylnaphthalene or partially oxidized derivative thereof in the presence of a catalyst comprising a bromine-containing component and at least one of a cobalt- or manganese-containing component.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 10060-32-9