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Phosphonic acid, (2-hydroxy-2-phenylpropyl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

187975-82-2

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187975-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 187975-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,9,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 187975-82:
(8*1)+(7*8)+(6*7)+(5*9)+(4*7)+(3*5)+(2*8)+(1*2)=212
212 % 10 = 2
So 187975-82-2 is a valid CAS Registry Number.

187975-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-hydroxy-2-phenylpropylphosphonate

1.2 Other means of identification

Product number -
Other names -

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:187975-82-2 SDS

187975-82-2Relevant academic research and scientific papers

Synthesis of β-hydroxyphosphonates by iron-catalyzed oxidative addition of phosphonyl radicals to alkenes

Taniguchi, Tsuyoshi,Idota, Atsushi,Yokoyama, Shin'Ichi,Ishibashi, Hiroyuki

experimental part, p. 4768 - 4770 (2011/10/02)

Phosphorohydrazidates have been shown to work as radical precursors by iron-catalyzed aerobic oxidation to generate corresponding phosphonyl radicals. Generated radicals cause intermolecular addition to various alkenes in the presence of molecular oxygen

A new entry to β-hydroxyphosphonates: The SmI2-mediated reaction of diethyl iodomethylphosphonate with carbonyl compounds

Orsini, Fulvia,Caselli, Alessandro

, p. 7255 - 7257 (2007/10/03)

In the presence of samarium iodide α-halophosphonates react with aliphatic carbonyl compounds (aldehydes and ketones) to afford β-hydroxyphosphonates in fairly good yields under neutral and mild conditions. Lower yields are obtained with aromatic carbonyl compounds.

A convenient (E)-stereoselective synthesis of alkenylphosphonates

Truel, Isabelle,Mohamed-Hachi, Abdourahman,About-Jaudet, Elie,Collignon, Noel

, p. 297 - 302 (2007/10/03)

Diethyl (E)-alkenylphosphonates have been prepared stereoselectively by dehydration of the corresponding β-hydroxyphosphonates using DCC/CuCl2 in refluxing toluene. Starting β-hydroxyphosphonates were obtained in high yield from diethyl methylphosphonate.

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