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1202186-22-8

8-(azidophenyl)triazolyl-O-trityl octahydroxamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1202186-22-8 Structure

  • Basic information

    1. Product Name: 8-(azidophenyl)triazolyl-O-trityl octahydroxamate
    2. Synonyms: 8-(azidophenyl)triazolyl-O-trityl octahydroxamate
    3. CAS NO:1202186-22-8
    4. Molecular Formula:
    5. Molecular Weight: 585.709
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1202186-22-8.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: 8-(azidophenyl)triazolyl-O-trityl octahydroxamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-(azidophenyl)triazolyl-O-trityl octahydroxamate(1202186-22-8)
    11. EPA Substance Registry System: 8-(azidophenyl)triazolyl-O-trityl octahydroxamate(1202186-22-8)

  • 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: 1202186-22-8(Hazardous Substances Data)

1202186-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1202186-22-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,1,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1202186-22:
(9*1)+(8*2)+(7*0)+(6*2)+(5*1)+(4*8)+(3*6)+(2*2)+(1*2)=98
98 % 10 = 8
So 1202186-22-8 is a valid CAS Registry Number.

1202186-22-8Downstream Products

1202186-22-8Relevant articles and documents

Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide

Canzoneri, Joshua C.,Chen, Po C.,Oyelere, Adegboyega K.

, p. 6588 - 6590 (2009)

We describe herein the synthesis and characterization of a new class of histone deacetylase (HDAC) inhibitors derived from conjugation of a suberoylanilide hydroxamic acid-like aliphatic-hydroxamate pharmacophore to a nuclear localization signal peptide. We found that these conjugates inhibited the histone deacetylase activities of HDACs 1, 2, 6, and 8 in a manner similar to suberoylanilide hydroxamic acid (SAHA). Notably, compound 7b showed a threefold improvement in HDAC 1/2 inhibition, a threefold increase in HDAC 6 selectivity and a twofold increase in HDAC 8 selectivity when compared to SAHA.

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