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56506-89-9

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56506-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56506-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56506-89:
(7*5)+(6*6)+(5*5)+(4*0)+(3*6)+(2*8)+(1*9)=139
139 % 10 = 9
So 56506-89-9 is a valid CAS Registry Number.

56506-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [Ph3P-CBr3]Br

1.2 Other means of identification

Product number -
Other names Tribrommethyl-triphenyl-phosphoniumbromid

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:56506-89-9 SDS

56506-89-9Downstream Products

56506-89-9Relevant articles and documents

Electrostatically-driven assembly of MWCNTs with a europium complex

Maggini, Laura,Traboulsi, Hassan,Yoosaf,Mohanraj, John,Wouters, Johan,Pietraszkiewicz, Oksana,Pietraszkiewicz, Marek,Armaroli, Nicola,Bonifazi, Davide

, p. 1625 - 1627 (2011)

Luminescent carbon-based materials have been prepared by electrostatic self-assembly of negatively-charged luminescent Eu(iii)-complex with imidazolium-functionalized MWCNTs.

Synthesis and Crystal Structure of Tribromomethyltriphenylphosphonium Bromide and Bis(tribromomethyltriphenylphosphonium) Tribromide Bromide

Vogt, H.,Frauendorf, C.,Fischer, A.,Jones, P. G.

, p. 223 - 228 (2007/10/02)

Tribromomethyltriphenylphosphonium bromide 1 has been prepared by the reaction of triphenylphosphine with tetrabromomethane in dichloromethane.Colourless crystals were obtained by recrystallization from the same solvent.The light-sensitive crystals change

NOVEL REACTIONS OF PHOSPHONIUM YLIDES WITH PERHALOALKANES: FIRST EXAMPLES OF HALOPHILIC ATTACKS BY PHOSPHONIUM YLIDES AND A FACILE ROUTE TO α-HALOALKYLPHOSPHONIUM SALTS

Li, Xing-Ya,Hu, Jin-Shan

, p. 6317 - 6320 (2007/10/02)

Phosphonium ylides Ph3=CHR (R = H, CH3, C2H5, n-C3H7, n-C5H11) react readily with perhalofluoroalkanes to afford regiospecifically α-haloalkylphosphonium salts Ph3P+-CHXR Y- (X = I, Br, Cl) in good yields.These reactions reveal a new type of reactivity phosphonium ylides, i.e., the halophilic attack on C-X bonds, and may be useful for the regiospecific synthesis of substituted haloolefins via Wittig reaction.

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