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Phosphorane, (3-methylbutylidene)triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39110-24-2

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39110-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39110-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,1 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39110-24:
(7*3)+(6*9)+(5*1)+(4*1)+(3*0)+(2*2)+(1*4)=92
92 % 10 = 2
So 39110-24-2 is a valid CAS Registry Number.

39110-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbutylidene(triphenyl)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Phosphorane,(3-methylbutylidene)triphenyl

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:39110-24-2 SDS

39110-24-2Relevant academic research and scientific papers

Allylic Selenides in Organic Synthesis: New Methods for the Synthesis of Allylic Amines

Shea, Regan G.,Fitzner, Jeffrey N.,Fankhauser, John E.,Spaltenstein, Andreas,Carpino, Philip A.,et al.

, p. 5243 - 5252 (2007/10/02)

Oxidative rearrangement of allylic selenides in the presence of various amine nucleophiles provides synthetic access to a variety of allylic amine derivatives.The stereochemical outcome of these reactions has been investigated, and is consistent with a -sigmatropic rearrangement mechanism.Several D-α-amino acids and racemic β,γ-unsaturated α-amino acids were prepared in this manner.A variant of this process employing an achiral allylic selenide and chiral amide afforded protected allylic amines in low diastereoisomeric excess.

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