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33143-92-9

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33143-92-9 Usage

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 6405, 1994 DOI: 10.1016/S0040-4039(00)78231-1

Check Digit Verification of cas no

The CAS Registry Mumber 33143-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33143-92:
(7*3)+(6*3)+(5*1)+(4*4)+(3*3)+(2*9)+(1*2)=89
89 % 10 = 9
So 33143-92-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO/c1-4-12(2,3)14-11-7-5-10(9-13)6-8-11/h1,5-8H,2-3H3

33143-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-methylbut-3-yn-2-yloxy)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-cyanophenyl 1,1-dimethylpropargyl ether

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:33143-92-9 SDS

33143-92-9Relevant articles and documents

Asymmetric epoxidation of chromenes mediated by iminium salts: Synthesis of mollugin and (3S,4R)-trans-3,4-dihydroxy-3,4-dihydromollugin

Bulman Page, Philip C.,Chan, Yohan,Noor Armylisas, Abu Hassan,Alahmdi, Mohammed

, p. 8406 - 8416 (2016/12/06)

Organocatalytic asymmetric epoxidation of chromenes mediated by iminium salt catalysts under non-aqueous conditions provided ees as high as 99%. Contrastingly, reaction under aqueous conditions can form the corresponding diol products with ees as high as 71%. The process has been used for the synthesis of the East African medicinal plant metabolite (3S,4R)-trans-3,4-dihydroxy-3,4-dihydromollugin.

Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes for the construction of trifluoromethylated heterocycles

Wang, Yanan,Jiang, Min,Liu, Jin-Tao

supporting information, p. 15315 - 15319 (2016/02/18)

A mild and efficient copper-catalyzed intramolecular carbotrifluoromethylation of alkynes has been achieved in the presence of Togni reagent as trifluoromethylating reagent. The reaction tolerates a range of substrates to give a group of trifluoromethylated heterocycles with high selectivities. A plausible mechanism was proposed on the basis of experimental results. And the Togni award goes to Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes is carried out with a Togni reagent as the trifluoromethylating reagent (see scheme). Various trifluoromethylated heterocycles are synthesized in moderate to good yields. Moreover, a range of common functional groups is tolerated under the reaction conditions.

Probing the stereoselectivity of P-glycoprotein - Synthesis, biological activity and ligand docking studies of a set of enantiopure benzopyrano[3,4-b] [1,4]oxazines

Jabeen, Ishrat,Wetwitayaklung, Penpun,Klepsch, Freya,Parveen, Zahida,Chiba, Peter,Ecker, Gerhard F.

scheme or table, p. 2586 - 2588 (2011/04/24)

A series of enantiomerically pure benzopyrano[3,4-b][1,4]oxazines have been synthesised and tested for their ability to inhibit P-glycoprotein. Reducing the conformational flexibility of the molecules leads to remarkable differences in the activity of dia

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