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1201937-85-0

C47H55N3O9S3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1201937-85-0 Structure

  • Basic information

    1. Product Name: C47H55N3O9S3
    2. Synonyms: C47H55N3O9S3
    3. CAS NO:1201937-85-0
    4. Molecular Formula:
    5. Molecular Weight: 902.166
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1201937-85-0.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: C47H55N3O9S3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C47H55N3O9S3(1201937-85-0)
    11. EPA Substance Registry System: C47H55N3O9S3(1201937-85-0)

  • 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: 1201937-85-0(Hazardous Substances Data)

1201937-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201937-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,9,3 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1201937-85:
(9*1)+(8*2)+(7*0)+(6*1)+(5*9)+(4*3)+(3*7)+(2*8)+(1*5)=130
130 % 10 = 0
So 1201937-85-0 is a valid CAS Registry Number.

1201937-85-0Upstream product

1201937-85-0Downstream Products

1201937-85-0Relevant articles and documents

Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds

Passarella, Daniele,Comi, Daniela,Vanossi, Andrea,Paganini, Gianfranco,Colombo, Francesco,Ferrante, Luca,Zuco, Valentina,Danieli, Bruno,Zunino, Franco

, p. 6358 - 6363 (2009)

Design and synthesis of an HDAC inhibitor and its merger with three tubulin binders to create releasable conjugate compounds is described. The biological evaluation includes: (a) in vitro reactivity with glutathione, (b) antiproliferative activity, (c) cell cycle analysis and (d) quantification of protein acetylation. The cellular pharmacology study indicated that the HDAC-inhibitor-drug conjugates retained antimitotic and proapoptotic activity with a reduced potency.

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