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405887-01-6

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405887-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 405887-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,8,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 405887-01:
(8*4)+(7*0)+(6*5)+(5*8)+(4*8)+(3*7)+(2*0)+(1*1)=156
156 % 10 = 6
So 405887-01-6 is a valid CAS Registry Number.

405887-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ({2-[(E)-2-(5-Carbamimidoyl-2-hydroxyphenyl)vinyl]-5-[(1-ethanimi doyl-4-piperidinyl)oxy]-2,3-dihydro-1H-indol-1-yl}sulfonyl)acetic acid

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:405887-01-6 SDS

405887-01-6Upstream product

405887-01-6Downstream Products

405887-01-6Relevant articles and documents

Cinnamylindoline derivatives: Synthesis and factor Xa (FXa) inhibitory activities

Noguchi, Tetsuji,Tanaka, Naoki,Nishimata, Toyoki,Goto, Riki,Hayakawa, Miho,Sugidachi, Atsuhiro,Ogawa, Taketoshi,Asai, Fumitoshi,Fujimoto, Koichi

, p. 1494 - 1504 (2008/12/23)

A series of cinnamylindoline derivatives were synthesized, and their factor Xa (FXa) inhibitory activities and selectivity over trypsin were evaluated. Among them, some novel derivatives showed potent FXa inhibitory activities and good selectivity over trypsin. Especially, (E)-2-{5-[1-(acetimidoyl)piperidin-4- yloxy]-2-[2-(5-amidino-2-hydroxyphenyl)ethen-1-yl]indolin-1-ylsulfonyl}acetic acid (22f) having 2-hydroxycinnamyl moiety exhibited the most potent FXa inhibitory activity in vitro. Furthermore, 22f also exhibited potent anticoagulant activities in vitro.

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