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12317-46-3

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12317-46-3 Usage

Uses

Different sources of media describe the Uses of 12317-46-3 differently. You can refer to the following data:
1. Dichloro(norbornadiene)palladium(II) can be useful starting material for the in situ preparation of a variety of chiral and achiral palladium catalysts.
2. Catalyst for:Aerobic kinetic resolution of secondary alcoholsKinetic oxidative resolution of 1-phenyl ethanolOxidative kinetic resolution-Claisen rearrangement sequenceAerobic oxidation of secondary alcohols

Check Digit Verification of cas no

The CAS Registry Mumber 12317-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,3,1 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 12317-46:
(7*1)+(6*2)+(5*3)+(4*1)+(3*7)+(2*4)+(1*6)=73
73 % 10 = 3
So 12317-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4.2ClH.Pd/c1-2-7-4-3-6(1)5-7;;;/h6-7H,5H2;2*1H;/q-4;;;+2/p-2

12317-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Norbornadiene PalladiuM(II) Dichloride

1.2 Other means of identification

Product number -
Other names Dichloro-2,5-norbornadiene Palladium(II)

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:12317-46-3 SDS

12317-46-3Relevant articles and documents

Thermal behaviour of polymers based on nadimides

Madan,Anand,Varma

, p. 531 - 539 (2008/10/08)

Carbocationic polymerization of N-ortho/meta/para tolyl-exo-norbornene dicarboximide (nadimide) was carried out using Pd(II) catalyst. Under similar conditions of polymerization, poly(N-m-tolyl nadimide) showed higher molecular mass compared to poly(N-p-tolyl nadimide) and poly(N-o-tolyl nadimide). Thermal stability of these polymers was evaluated by dynamic thermogravimetry in nitrogen atmosphere. The polymers were stable up to 460 °C and lost mass above this temperature in a single step. The characteristic decomposition temperature and char yield of these polymers were higher than the polymers prepared by using ring opening metathesis polymerization. The difference has been attributed to the presence of rigid bicyclic ring structure in these polymers.

A vibrational study of the metal-olefin bond in norbornadiene complexes of Rh(I), Pd(II) and Pt(II)

Wertz, D. W.,Moseley, M. A.

, p. 467 - 472 (2007/10/02)

Vibrational assignments of the complexes 2, PtCl2C7H8, and PdCl2C7H8 have been undertaken.A reinvestigation of the norbornadiene spectrum was necessary and a new set of assignments is given.The shift in energy of bands I and II and the out-of-plane olefinic C-H wagging modes, as well as the relative energies of the bands associated with the metal-olefin motions are consistent with the total metal-norbornadiene interaction following the order Rh > Pt > Pd and the excent of the ? component being ordered as Rh ca/= Pt > Pd.

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