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4-phenyl-3-penten-1-yl iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109900-90-5

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109900-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109900-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109900-90:
(8*1)+(7*0)+(6*9)+(5*9)+(4*0)+(3*0)+(2*9)+(1*0)=125
125 % 10 = 5
So 109900-90-5 is a valid CAS Registry Number.

109900-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyl-3-penten-1-yl iodide

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:109900-90-5 SDS

109900-90-5Relevant academic research and scientific papers

Chiral Selenide-Catalyzed Enantioselective Allylic Reaction and Intermolecular Difunctionalization of Alkenes: Efficient Construction of C-SCF3 Stereogenic Molecules

Liu, Xiang,Liang, Yaoyu,Ji, Jieying,Luo, Jie,Zhao, Xiaodan

supporting information, p. 4782 - 4786 (2018/04/17)

New approaches for the synthesis of enantiopure trifluoromethylthiolated molecules by chiral selenide-catalyzed allylic trifluoromethylthiolation and intermolecular difunctionalization of unactivated alkenes are disclosed. In these transformations, functi

Cyclopentane ring formation in the cycloaddition reaction of 3-alkenyl radicals to radicophilic olefins

Saiic, Radomir N.,Cekovic, Zivorad

, p. 3627 - 3640 (2007/10/02)

Regioselective additions of 3-alkenyl radicals (10 and 20) to electron deficient olefinic bonds (7 and 17), followed by intramolecular 5- exo-cyclization and repeated addition to radicophilic double bonds were investigated and combined into a sequence of

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