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405887-83-4

C21H31F3N2O5Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 405887-83-4 Structure

  • Basic information

    1. Product Name: C21H31F3N2O5Si
    2. Synonyms:
    3. CAS NO:405887-83-4
    4. Molecular Formula:
    5. Molecular Weight: 476.568
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 405887-83-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C21H31F3N2O5Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H31F3N2O5Si(405887-83-4)
    11. EPA Substance Registry System: C21H31F3N2O5Si(405887-83-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 405887-83-4(Hazardous Substances Data)

405887-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 405887-83-4 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, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 405887-83:
(8*4)+(7*0)+(6*5)+(5*8)+(4*8)+(3*7)+(2*8)+(1*3)=174
174 % 10 = 4
So 405887-83-4 is a valid CAS Registry Number.

405887-83-4Downstream Products

405887-83-4Relevant 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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