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105785-75-9

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105785-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105785-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,7,8 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105785-75:
(8*1)+(7*0)+(6*5)+(5*7)+(4*8)+(3*5)+(2*7)+(1*5)=139
139 % 10 = 9
So 105785-75-9 is a valid CAS Registry Number.

105785-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2,2-dimethylpropoxy)-triphenyl-λ<sup>5</sup>-phosphane

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:105785-75-9 SDS

105785-75-9Downstream Products

105785-75-9Relevant articles and documents

Development of a redox-free Mitsunobu reaction exploiting phosphine oxides as precursors to dioxyphosphoranes

Tang, Xiaoping,Chapman, Charlotte,Whiting, Matthew,Denton, Ross

supporting information, p. 7340 - 7343 (2014/07/07)

The development of the first redox-free protocol for the Mitsunobu reaction is described. This has been achieved by exploiting triphenylphosphine oxide-the unwanted by-product in the conventional Mitsunobu reaction-as the precursor to the active P(v) coupling reagent. Multinuclear NMR studies are consistent with hydroxyl activation via an alkoxyphosphonium salt.

Bis(neopentyloxy)triphenylphosphorane: A Versatile, Nonalkylating Cyclodehydration Reagent

Kelly, Jeffery W.,Evans, Slayton A.

, p. 5490 - 5492 (2007/10/02)

Bis(neopentyloxy)triphenylphosphorane (BNTP; 31P δ -58.3) is prepared in 48percent yield by reaction of 2 equiv of lithium neopentoxide with dibromotriphenylphosphorane in anhydrous dichloromethane from -78 to 25 deg C.BNTP smoothly converts a variety of diols, 2-aminoethanol, and 4-mercaptobutanol to the corresponding heterocycles in excellent yields (>95percent) by 13C and 31P NMR analysis.

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