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1745-15-9

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1745-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1745-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1745-15:
(6*1)+(5*7)+(4*4)+(3*5)+(2*1)+(1*5)=79
79 % 10 = 9
So 1745-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H17Cl/c1-3-4-5-6-7-8-9(2)10/h2-8H2,1H3

1745-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloronon-1-ene

1.2 Other means of identification

Product number -
Other names 2-chloro-non-1-ene

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:1745-15-9 SDS

1745-15-9Downstream Products

1745-15-9Relevant articles and documents

Partial Reduction and Selective Transfer of Hydrogen Chloride on Catalytic Gold Nanoparticles

Oliver-Meseguer, Judit,Doménech-Carbó, Antonio,Boronat, Mercedes,Leyva-Pérez, Antonio,Corma, Avelino

supporting information, p. 6435 - 6439 (2017/05/29)

HCl in solution accepts electron density from Au NPs and partially reduces at room temperature, as occurs with other simple diatomic molecules, such as O2 and H2. The activation can be run catalytically in the presence of alkynes to give exclusively E-vinyl chlorides, after the regio- and stereoselective transfer of HCl. Based also on this method, vinyl chloride monomer (VCM) can be produced in a milder and greener way than current industrial processes.

ADDITION DE L'ACIDE THIOCYANIQUE AUX ACETYLENIQUES A L'AIDE DE Hg(II)-I. ADDITION DU GROUPEMENT SCN(1-) EN PRESENCE D'UN ACIDE FORT

Giffard, Michel,Cousseau, Jack,Gouin, Lucien,Crahe, Marie-Renee

, p. 801 - 810 (2007/10/02)

Mercury(II) thiocyanate Hg(SCN)2 catalyses thiocyanic acid HSCN addition to unactivated acetylenic compounds R1-CC-R2.Bonding of the SCN moiety to carbon occurs through sulphur or nitrogen depending upon the influence of R1 and R2; vinyl thiocyanates NCS-C(R1)=CH2 are obtained specifically from terminal acetylenic compounds but some symmetrically disubstituted alkynes may afford vinyl isothiocyanates SCN-C(R1)=CH-R2 ( R1=R2=Et, n-Bu ).A simple preparation of tetraphenylphosphonium hydrogen dithiocyanate Ph4P(1+)*(1-) is reported.

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