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88708-58-1

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88708-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88708-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,0 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88708-58:
(7*8)+(6*8)+(5*7)+(4*0)+(3*8)+(2*5)+(1*8)=181
181 % 10 = 1
So 88708-58-1 is a valid CAS Registry Number.

88708-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (2-benzyl-2-hydroxy-3-phenyl)propylphosphonate

1.2 Other means of identification

Product number -
Other names dimethyl 2,2-dibenzyl-2-hydroxyethylphosphonate

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:88708-58-1 SDS

88708-58-1Relevant articles and documents

The Olefin Synthesis from β-Hydroxyalkylphosphonates Induced by Fluorides or Relatively Weak Bases

Kawashima, Takayuki,Ishii, Takafumi,Inamoto, Naoki,Tokitoh, Norihiro,Okazaki, Renji

, p. 209 - 219 (1998)

β-Hydroxyalkylphosphonates, which were prepared readily from alkylphosphonates and carbonyl compounds, were treated with a fluoride ion such as CsF or with relatively weak bases such as K2CO3 in N,N-dimethylformamide to give the corresponding olefins in good yields. One molar equivalent of water to bases is effective for increasing the yields of olefins. The stereochemistry of erythro-dimethyl (2-hydroxy-1-methyl-2-phenyl)ethylphosphonate was determined by X-ray crystallographic analysis. Use of threo-isomer gave (E)-olefin exclusively, while that of erythro-enricned isomer afforded predominantly (Z)-olefin, indicating that the present olefination proceeds stereospecifically in a manner of syn-elimination.

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