Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13041-10-6

Post Buying Request

13041-10-6 Suppliers

Recommended suppliersmore

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

13041-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13041-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13041-10:
(7*1)+(6*3)+(5*0)+(4*4)+(3*1)+(2*1)+(1*0)=46
46 % 10 = 6
So 13041-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-9-8-6-2-3-7(8)5-4-6/h2-3,6-8H,4-5H2,1H3

13041-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name anti-7-methoxy-Bicyclo(2.2.1)hept-2-ene

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:13041-10-6 SDS

13041-10-6Downstream Products

13041-10-6Relevant articles and documents

Rh(III)-photosensitized interconversion of norbornadiene and quadricyclane

Sluggett, Gregory W.,Turro, Nicholas J.,Roth, Heinz D.

, p. 8834 - 8838 (2007/10/03)

The utility of two Rh(III) diimine complexes, Rh(phen)33+ and Rh(phi)2(phen)3+ (phen = 1,10-phenanthroline, phi = 9,10-phenanthrenequinone diimine), as sensitizers for the interconversion of norbornadiene (N) and quadricyclane (Q) has been investigated using steady-state photochemical and laser flash photolysis (LFP) techniques. Irradiation of acetonitrile solutions of Rh(phen)33+ and N causes slow conversion to Q. The reaction is reversible; irradiation of Rh(phen)33+ in the presence of Q leads to N. Irradiation of acetonitrile solutions of Rh(phi)2(phen)3+ and Q yields N. However, this reaction is irreversible; irradiation of the Rh-(III) complex in the presence of N fails to afford Q. Irradiation of methanol solutions of either Rh(III) complex in the presence of N or Q affords minor amounts of two methanol-C7 adducts but fails to quench the N-Q interconversion reaction. The results are consistent with N-Q interconversion via an exciplex intermediate. The Rh(III)-sensitized deazatization of two cyclic azoalkane derivatives (Azo-N, Azo-Q) of N and Q was also investigated. Deazatization was achieved by Rh(phen)33+ but not Rh(phi)2(phen)3+ sensitization. The results are consistent with a mechanism involving triplet energy transfer, but the involvement of exciplex intermediates cannot be ruled out. Bimolecular rate constants for quenching of the Rh(III) excited states by N, Q, Azo-N, and Azo-Q were determined by LFP.

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

What can I do for you?
Get Best Price

Get Best Price for 13041-10-6