Welcome to LookChem.com Sign In|Join Free
  • or
Benzoic acid, 2-[2-(1-naphthalenyl)ethenyl]-, methyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90340-67-3

Post Buying Request

90340-67-3 Suppliers

Recommended suppliers

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

90340-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90340-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90340-67:
(7*9)+(6*0)+(5*3)+(4*4)+(3*0)+(2*6)+(1*7)=113
113 % 10 = 3
So 90340-67-3 is a valid CAS Registry Number.

90340-67-3SDS

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 methyl 2-[(E)-2-(1-naphthyl)ethenyl]benzoate

1.2 Other means of identification

Product number -
Other names -

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:90340-67-3 SDS

90340-67-3Relevant academic research and scientific papers

Selenium-mediated synthesis of biaryls through rearrangement

Shahzad, Sohail A.,Vivant, Clotilde,Wirth, Thomas

supporting information; experimental part, p. 1364 - 1367 (2010/06/17)

"Chemical Equation Presented" A new cyclization of β-keto ester substituted stilbene derivatives using selenium electrophiles in the presence of Lewis acids is described. Substituted naphthols are obtained through cyclization and subsequent 1,2-rearrangement of aryl groups under very mild reaction conditions.

Diselenide- and disulfide-mediated synthesis of isocoumarins

Shahzad, Sohail A.,Venin, Claire,Wirth, Thomas

experimental part, p. 3465 - 3472 (2010/09/07)

Cyclizations of stilbenecarboxylic acids to the corresponding isocoumarin derivatives using diselenide or disulfide reagents have been developed. By employing bis(triflouroacetoxy)iodobenzene as oxidant for the 6-endo-trig cyclizations a variety of dihydroisocoumarins have been prepared in good yields. This method is capable of forming isocoumarins and dihydroisocoumarin derivatives by a cyclization-elimination route.

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 90340-67-3