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28240-68-8

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28240-68-8 Usage

Chemical Properties

Clear colorless to pale yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 28240-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,4 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28240-68:
(7*2)+(6*8)+(5*2)+(4*4)+(3*0)+(2*6)+(1*8)=108
108 % 10 = 8
So 28240-68-8 is a valid CAS Registry Number.
InChI:InChI=1/CH2Cl4P2/c2-6(3)1-7(4)5/h1H2

28240-68-8 Well-known Company Product Price

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  • Aldrich

  • (451053)  Bis(dichlorophosphino)methane  95%

  • 28240-68-8

  • 451053-1G

  • 766.35CNY

  • Detail

28240-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methylenebis(dichlorophosphine) Methylenebis(phosphonous dichloride)

1.2 Other means of identification

Product number -
Other names Bis(dichlorophosphino)methane

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:28240-68-8 SDS

28240-68-8Relevant articles and documents

Novel Phosphonylphosphinyl (P-C-P-C-) Analogues of Biochemically Interesting Diphosphates. Syntheses and Properties of P-C-P-C- Analogues of Isopentenyl Diphosphate and Dimethylallyl Diphosphate

McClard, Ronald W.,Fujita, Thomas S.,Stremler, Kay E.,Poulter, C. Dale

, p. 5544 - 5545 (1987)

-

Design and synthesis of phosphonate inhibitors of glutamine synthetase

Farrington,Kumar,Wedler

, p. 2062 - 2067 (2007/10/02)

Inhibitors 1-4 have been shown previously to undergo enzymatic phosphorylation by glutamine synthetase (GS). Phosphonates 6-9 were designed as chemically stable analogues of these phosphorylated inhibitors, incorporating either a tetrahedral sulfur group

LINEARE OLIGOPHOSPHAALKANE XIII.TRIPHOSPHAALKANE MIT DEM P-C-P-C-P-DONORSKELETT; LIGANDEN FUER DEN AUFBAU VON MEHRKERNKOMPLEXEN

Brauer, David J.,Hietkamp, Sibbele,Sommer, Herbert,Stelzer, Othmar,Mueller, Gerhard,et al.

, p. 411 - 434 (2007/10/02)

The triphosphaalkane Cl2PCH2PClCH2PCl2 (III) is formed as a by-product in the synthesis of Cl2PCH2PCl2 (II).On treating III with MeMgCl or EtOH (in the presence of a base), the methyl or ethoxy derivative (V or VI) may be obtained in satisfactory yields.With Ni(CO)4 or Fe2(CO)9 V forms trinuclear complexes nM>PMe2CH2PMen>CH2PMe2n> (X, XIII; M = Fe, Ni; n = 4, 3) or binuclear stable six-membered chelate ring systems n>PMe(CH2PMe2)2m> (IX, XIV; M = Fe, Ni; n = 4, 3; m = 3, 2).An excess of Fe2(CO)9 (molar ratio V/Fe2(CO)9 1/5) yields XI with an Fe-Fe bond or the cluster XII, respectively.In both cases V bridges the Fe-Fe bond with a P-C-P donor set.X-ray structural analysis of X (triclinic, space group P1) exhibits a staggered arrangement of the three metal carbonyl fragments bound to the "stretched" P-C-P-C-P skeleton of V (Fe(1)-P(1) 2.236(1), Fe(2)-P(2) 2.226(1), Fe(3)-P(3) 2.231(1) Angstroem, P(1)-C(13)-P(2) 126.7(1), P(2)-C(14)-P(3) 127.6(1) deg).In XI (monoclinic, space group P21/n) one P-C-P donor set together with the two iron atoms Fe(2) and Fe(3) form a stable five-membered Fe2P2C ring (Fe(2)-Fe(3) 2.705(1), Fe(2)-P(2) 2.251(1), Fe(3)-P(3) 2.239(1) Angstroem).The third phosphorus atom P(1) binds an Fe(CO)4 group (Fe(1)-P(1) 2.245(1) Angstroem).The structure of cluster compound XII (monoclinic, space group P21/n) is derived from that of Os3(CO)12.One P-C-P donor set of V replaces two CO groups in equatorial positions, forming a stable Fe2P2C five-membered ring.The remaining donor position of V coordinates with an Fe(CO)4 group.

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