Welcome to LookChem.com Sign In|Join Free
  • or
Spiro[9H-fluorene-9,5'-[1,4,2]oxaselenazole], 3'-(2,4,6-trimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114263-85-3

Post Buying Request

114263-85-3 Suppliers

Recommended suppliers

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

114263-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114263-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,6 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114263-85:
(8*1)+(7*1)+(6*4)+(5*2)+(4*6)+(3*3)+(2*8)+(1*5)=103
103 % 10 = 3
So 114263-85-3 is a valid CAS Registry Number.

114263-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,4,6-trimethylphenyl)spiro[1,4,2-oxaselenazole-5,9'-fluorene]

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:114263-85-3 SDS

114263-85-3Downstream Products

114263-85-3Relevant academic research and scientific papers

SELENOFLUORENONE: SYNTHESIS AND CYCLOADDITION CHEMISTRY

Meinke, Peter T.,Krafft, Grant A.,Spencer, James T.

, p. 3887 - 3890 (1987)

Selenofluorenone, prepared from fluorenyl selenocyanate by base-induced elimination, participates efficiently in Diels-Alder cycloaddition and 1,3-dipolar cycloaddition reactions.

Preparation and Cycloaddition Reactions of Selenoketones

Meinke, Peter T.,Krafft, Grant A.

, p. 8679 - 8685 (2007/10/02)

Dienophilic selenoketones have been prepared by base-induced elimination of cyanide from selenocyanates containing electron-withdrawing or conjugating substituents.Cycloaddition reactions of selenoketones with dienes or dipolar reagents proceed efficientl

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 114263-85-3