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102532-71-8

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102532-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102532-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102532-71:
(8*1)+(7*0)+(6*2)+(5*5)+(4*3)+(3*2)+(2*7)+(1*1)=78
78 % 10 = 8
So 102532-71-8 is a valid CAS Registry Number.
InChI:InChI=1/2C26H22P2.ClH.Cu/c2*1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;;/h2*1-22H;1H;/q;;;+1/p-1/b2*22-21-;;

102532-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name copper(1+),[(Z)-2-diphenylphosphanylethenyl]-diphenylphosphane,chloride

1.2 Other means of identification

Product number -
Other names (Cu(cis-Ph2PCHCHPPh2)2)Cl

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:102532-71-8 SDS

102532-71-8Downstream Products

102532-71-8Relevant articles and documents

Copper(I) complexes with bidentate tertiary phosphine ligands: Solution chemistry and antitumor activity

Berners-Price, Susan J.,Johnson, Randall K.,Mirabelli, Christopher K.,Faucette, Leo F.,McCabe, Francis L.,Sadler, Peter J.

, p. 3383 - 3387 (2008/10/08)

Copper may play an important role in the antitumor activity of diphosphines. The tetrahedral bischelated copper(I) complexes [Cu(dppey)2]Cl and [Cu(dppp)2]Cl, where dppey is Ph2PCH=CHPPh2 and dppp is Ph2P(CH2)3PPh2, were synthesized and characterized. The bridged dicopper(I) complex (CuCl)2(dppe)3, where dppe is Ph2P(CH2)2PPh2, underwent dissociative equilibria in CDCl3 and CD2Cl2 solutions, as determined by temperature-dependent 1H and 31P NMR studies. One of the products was [Cu(dppe)2]+, the proportion of which increased on adding excess dppe. The complex was also a product from the reaction of Cu2+ with excess dppe in DMA. The complexes [Cu(P-P)2]Cl, where P-P is dppey or dppp, and (CuCl)2(dppe)3 were all active against P388 leukemia, M5076 reticulum cell sarcoma, and B16 melanoma. [Cu(eppe)2]Cl, where eppe is Et2P(CH2)2PPh2, was active only against P388 leukemia. The activities were comparable to those of the analogous Au(I) complexes, and complexes were more potent than the free ligands.

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