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93790-54-6

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93790-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93790-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93790-54:
(7*9)+(6*3)+(5*7)+(4*9)+(3*0)+(2*5)+(1*4)=166
166 % 10 = 6
So 93790-54-6 is a valid CAS Registry Number.

93790-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-iodophenoxy)-N,N-dimethylethanamine

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:93790-54-6 SDS

93790-54-6Relevant articles and documents

Incorporation of histone deacetylase inhibitory activity into the core of tamoxifen – A new hybrid design paradigm

Palermo, Anthony F.,Diennet, Marine,El Ezzy, Mohamed,Williams, Benjamin M.,Cotnoir-White, David,Mader, Sylvie,Gleason, James L.

supporting information, p. 4428 - 4440 (2018/08/06)

Hybrid antiestrogen/histone deacetylase (HDAC) inhibitors were designed by appending zinc binding groups to the 4-hydroxystilbene core of 4-hydroxytamoxifen. The resulting hybrids were fully bifunctional, and displayed high nanomolar to low micromolar IC

Synthesis and growth inhibition activity of fluorinated derivatives of tamoxifen

Malo-Forest, Bianca,Landelle, Grégory,Roy, Jessye-Ann,Lacroix, Jacques,Gaudreault, René C.,Paquin, Jean-Fran?ois

, p. 1712 - 1715 (2013/03/29)

The design and synthesis of 11 fluorinated derivatives of tamoxifen are described. Growth inhibition values (GI50) on human HT-29, M21, MCF7, and MDA-MB-231 tumor cells are also reported. In general, the GI50 values are similar or sl

Zirconocene-mediated highly regio- and stereoselective synthesis of multisubstituted olefins starting from 1-alkynylboronates

Nishihara, Yasushi,Miyasaka, Mitsuru,Okamoto, Masanori,Takahashi, Hideki,Inoue, Eiji,Tanemura, Kenki,Takagi, Kentaro

, p. 12634 - 12635 (2008/03/13)

Multisubstituted olefins are efficiently prepared by the zirconocene-mediated regio- and stereoselective coupling between 1-alkynylboronates and ethylene, followed by sequential transformation in moderate to high yields. The proper combination of substrates and reaction conditions is important for high yields. The synthesis of various tetrasubstituted alkenes in a regio- and stereocontrolled manner is described. This methodology has been applied to the synthesis of (Z)-tamoxifen in a concise, regio- and stereoselective manner. This multicomponent coupling strategy involves the characteristics of 1-alkynylboronates toward high selectivities followed by palladium(0)-mediated cross-coupling with aryl halides. Copyright

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