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toluene-4-sulfonic acid 2-(3H-inden-1'-yl)-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170633-72-4

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170633-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170633-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,6,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 170633-72:
(8*1)+(7*7)+(6*0)+(5*6)+(4*3)+(3*3)+(2*7)+(1*2)=124
124 % 10 = 4
So 170633-72-4 is a valid CAS Registry Number.

170633-72-4Downstream Products

170633-72-4Relevant academic research and scientific papers

Selective alkylation and Suzuki coupling as an efficient strategy for introducing functional anchors to the ethylene-bis(indenyl) ligand

Panarello, Anthony P.,Vassylyev, Oleksiy,Khinast, Johannes G.

, p. 1353 - 1356 (2007/10/03)

Chiral ansa-ethylene-bis(indenyl)-metal complexes, EBI-MX2, are useful pre-catalysts for a wide variety of reactions, including hydrogenations, hydrosilylations, and polymerization reactions. In order to immobilize these complexes onto heterogeneous supports, a new methodology was developed to introduce functional anchors to the ethylene-bis(indenyl) ligand, EBI. This was accomplished by selective alkylation of indene to form toluene-4-sulfonic acid 2-(3H-inden-1-yl)-ethyl ester, which was then used to alkylate 6-bromoindene. The selective introduction of an aryl bromide then undergoes coupling reactions with aryl borates via the Suzuki coupling to efficiently introduce an alkenyl or alcohol, functional anchor in a simple four step synthesis.

1-[2-(1H-INDEN-3-YL)ETHYL]-4-(NAPHTH-1-YL)PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN THERAPEUTICS

-

, (2008/06/13)

Compounds of formula: STR1 in which X represents a hydrogen atom, a C 1-C 3 alkoxy group or a cyclopropylmethoxy group and Y represents a hydrogen atom or a methoxy group, are useful in the therapy of conditions.

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