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Benzene, [[(1-ethyl-2-iodo-1-butenyl)thio]methyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112701-55-0

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112701-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112701-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112701-55:
(8*1)+(7*1)+(6*2)+(5*7)+(4*0)+(3*1)+(2*5)+(1*5)=80
80 % 10 = 0
So 112701-55-0 is a valid CAS Registry Number.

112701-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-benzylthio-4-iodohex-3-ene

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:112701-55-0 SDS

112701-55-0Downstream Products

112701-55-0Relevant academic research and scientific papers

Stereoselective Bifunctionalization of Alkynes by Means of the Mercury(II) Salt-Iodine Combination

Barluenga, Jose,Martinez-Gallo, Jose M.,Najera, Carmen,Yus, Miguel

, p. 1017 - 1020 (2007/10/02)

The reaction of alkynes with iodine and mercury(II) salts (chloride, acetate, methanesulphonate, toluene-p-sulphonate, benzylsulphide, toluene-p-sulphinate, and thiocyanate) affords stereoselectively E-β-functionalized vinyl iodides resulting from the ionic addition of iodine and the mercury(II) salt anion.Unsymmetrical alkynes yield regiospecifically Markovnikov addition products.In the case of mercury(II) thiocyanate the reaction can be used also for the stereoselective preparation of E-1,2-dithiocyanatoalkenes.An ionic mechanism is proposed according to the observed regio- and stereochemistry.

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