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Benzene, [(1-ethenylbutyl)seleno]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90036-67-2

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90036-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90036-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90036-67:
(7*9)+(6*0)+(5*0)+(4*3)+(3*6)+(2*6)+(1*7)=112
112 % 10 = 2
So 90036-67-2 is a valid CAS Registry Number.

90036-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-1-en-3-ylselanylbenzene

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:90036-67-2 SDS

90036-67-2Relevant academic research and scientific papers

Iridium-catalyzed allylic alkylations of sodium phenyl selenide

Cui, Ruimin,Guo, Xinwen,Zheng, Shengcai,Zhao, Xiaoming

, p. 2647 - 2651 (2013/01/15)

An iridium-catalyzed allylic substitution of sodium phenyl selenide with unsymmetrical allyl carbonates was accomplished, which produced the linear allyl phenyl selenides in 38%-74% yields. An asymmetric iridium-catalyzed allylation of sodium phenyl selen

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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