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Bis(2-(carbomethoxy)ethyl)phenylphosphine is a complex organic compound with the chemical formula C13H17O4P. It is a colorless liquid at room temperature and is soluble in organic solvents. This phosphine derivative features a phenyl group attached to a phosphorus atom, with two ethyl groups, each containing a carbomethoxy (ester) group, bonded to the phosphorus. The compound is used as a reagent in organic synthesis, particularly in the formation of phosphorus-containing compounds and as a ligand in transition metal catalysis. Its stability and reactivity make it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals.

6775-11-7

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6775-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6775-11-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6775-11:
(6*6)+(5*7)+(4*7)+(3*5)+(2*1)+(1*1)=117
117 % 10 = 7
So 6775-11-7 is a valid CAS Registry Number.

6775-11-7SDS

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 bis(2-(carbomethoxy)ethyl)phenylphosphine

1.2 Other means of identification

Product number -
Other names 3,3'-phenylphosphanediyl-bis-propionic acid dimethyl ester

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:6775-11-7 SDS

6775-11-7Relevant academic research and scientific papers

A Commercially Available Ruthenium Compound for Catalytic Hydrophosphination

Cibuzar, Michael P.,Dannenberg, Steven G.,Waterman, Rory

, p. 446 - 451 (2019/08/26)

Hydrophosphination with a commercially available ruthenium compound, bis(cyclopentadienylruthenium dicarbonyl) dimer ([CpRu(CO)2]2), was explored. Styrene derivatives or Michael acceptors react readily with either primary or secondar

Hydrophosphination of alkenes and alkynes with primary phosphines catalyzed by zirconium complexes bearing aminophenolato ligands

Zhang, Yu,Wang, Xinxin,Wang, Yaorong,Yuan, Dan,Yao, Yingming

supporting information, p. 9090 - 9095 (2018/07/25)

Zirconium complexes stabilized by amine-bridged bis(phenolato) ligands showed good activity and chemo-selectivity in catalyzing intermolecular hydrophosphination of C-C multiple bonds with primary phosphines under mild conditions. A broad range of alkenes

Methods of and compositions for reducing neuronal cell death

-

Page/Page column 5, (2008/06/13)

Methods and compositions involving a class of boron-protected phenylphosphine agents having increased cell permeability and having improved chemical stability for treating or for preventing neuronal cell death-related diseases or conditions in a human or

Synthesis of Tridentate Phosphine Ligands RP2 (Y = OR' or CO2R', n = 1 or 2) and Some Bidentate Chiral Phosphines R2PCH(CH3)CO2Me

Wolfsberger, Werner,Bank, Juergen,Werner, Helmut

, p. 1319 - 1328 (2007/10/03)

The bis(γ-alkoxypropyl)phosphines RP(CH2CH2OR')2 1-4 were prepared by the reaction of RPLi2 (generated by lithiation of RPH2 with n-BuLi) with ClCH2CH2OR'.Deprotonation of the alkyl group R of RPH2 by n-BuLi and other side reactions leading preferably to

Carbon-Phosphorus Heterocycles. Synthesis of Phosphorus-Containing Cannabinoid Precursors and a Single-Crystal Analysis of 1,2,3,4-Tetrahydro-10-hydroxy-8-n-pentyl-5H-phosphorinobenzopyran-5-one 3-Oxide

Rampal, Jang B.,Berlin, K. Darrell,Pantaleo, Nantelle S.,McGuffy, Ann,Helm, Dick van der

, p. 2032 - 2036 (2007/10/02)

The synthesis of 1,2,3,4-tetrahydro-10-hydroxy-8-methyl- and 1,2,3,4-tetrahydro-10-hydroxy-8-n-pentyl-3-phenyl-5H-phosphorinobenzopyran-5-one 3-oxide have been achieved.These precursors of cannabinoid analogues are the first reported in this fam

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