Welcome to LookChem.com Sign In|Join Free
  • or
dimethyl cycloocta-1,3,5,7-tetraene-1,2-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15956-91-9

Post Buying Request

15956-91-9 Suppliers

Recommended suppliers

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

15956-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15956-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,5 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15956-91:
(7*1)+(6*5)+(5*9)+(4*5)+(3*6)+(2*9)+(1*1)=139
139 % 10 = 9
So 15956-91-9 is a valid CAS Registry Number.

15956-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (1Z,3Z,5Z,7Z)-cycloocta-1,3,5,7-tetraene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1,2-dicarbomethoxycyclooctatetraene

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:15956-91-9 SDS

15956-91-9Relevant academic research and scientific papers

Acid and Polarity Effects in Benzene Photoreactions with Alkenes and Alkynes

Bryce-Smith, D.,Gilbert, A.,Al-Jalal, N.,Deshpande, R.R.,Grzonka, J.,et al.

, p. 1101 - 1112 (2007/10/02)

The effects of polar solvents and proton donors on various photoreactions of the benzene ring with electron-acceptor alkenes and alkynes are described and discussed in relation to the various electronic excitation mechanisms involved.Proton donors prove valuable as mechanistic probes for polar intermediates in such processes, and can in some systems both initiate and divert reaction pathways. - Key words: Photoreactions, Benzene, Alkenes, Alkynes, Acid Effects

PHOTOFRAGMENTATION OF OXAZOLIDINES. A NEW METHOD FOR THE GENERATION OF AZIRIDINES

Tsuge, Otohiko,Oe, Koji,Kawaguchi, Noriyuki

, p. 1585 - 1588 (2007/10/02)

Irradiation of 4,5-cis-2,3,4,5-tetraaryloxazolidines and 3-aryl-3a,9b-dihydro-acenaphthoxazolidines generates the corresponding aziridine intermediates with elimination of aldehyde formed by fission of the C2-O and C4-C5 bonds in the former and the C2-O and C2-N bonds int the latter, respectively.The intervention of aziridine intermediates was proved by photo-cycloadditions.

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 15956-91-9