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ethyl 2-(4-{[(2S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl]methoxy}phenyl)-3-(5-cyano-1-benzothien-2-yl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

701305-53-5

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701305-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 701305-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,1,3,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 701305-53:
(8*7)+(7*0)+(6*1)+(5*3)+(4*0)+(3*5)+(2*5)+(1*3)=105
105 % 10 = 5
So 701305-53-5 is a valid CAS Registry Number.

701305-53-5Downstream Products

701305-53-5Relevant academic research and scientific papers

Design, synthesis and biological activity of amidinobicyclic compounds (derivatives of DX-9065a) as factor Xa inhibitors: SAR study of S1 and aryl binding sites

Komoriya, Satoshi,Kanaya, Naoaki,Nagahara, Takayasu,Yokoyama, Asako,Inamura, Kazue,Yokoyama, Yukio,Katakura, Shin-Ichi,Hara, Tsuyoshi

, p. 2099 - 2114 (2007/10/03)

Since factor Xa (fXa) plays a pivotal role in the blood coagulation cascade, inhibition of fXa is thought to be an effective treatment for a variety of thrombotic events. (2S)-2-[4-[[(3S)-1-Acetimidoyl-3-pyrrolidinyl]oxy]phenyl] -3-(7-amidino-2-naphthyl)p

AROMATIC AMIDINE DERIVATIVES AND SALTS THEREOF

-

, (2008/06/13)

An anticoagulant agent which comprises, as an active ingredient, an aromatic amidine derivative represented by the following general formula (1) or a salt thereof: STR1 wherein the group represented by STR2 is a group selected from indolyl, benzofuranyl, benzothienyl, benzimidazolyl, benzoxazolyl, benzothiazolyl, naphthyl, tetrahydronaphthyl and indanyl; X is a single bond, an oxygen atom, a sulfur atom or a carbonyl group; and Y is a saturated or unsaturated 5-or 6-membered heterocyclic moiety or cyclic hydrocarbon moiety optionally having a substituent group, an amino group optionally having a substituent group or an aminoalkyl group optionally having a substituent group.The inventive compound has a high anticoagulant capacity based on its excellent FXa inhibition activity.

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