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858343-03-0

C35H22N2O11 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 858343-03-0 Structure

  • Basic information

    1. Product Name: C35H22N2O11
    2. Synonyms: C35H22N2O11
    3. CAS NO:858343-03-0
    4. Molecular Formula:
    5. Molecular Weight: 646.566
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 858343-03-0.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: C35H22N2O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C35H22N2O11(858343-03-0)
    11. EPA Substance Registry System: C35H22N2O11(858343-03-0)

  • 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: 858343-03-0(Hazardous Substances Data)

858343-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858343-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,3,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 858343-03:
(8*8)+(7*5)+(6*8)+(5*3)+(4*4)+(3*3)+(2*0)+(1*3)=190
190 % 10 = 0
So 858343-03-0 is a valid CAS Registry Number.

858343-03-0Downstream Products

858343-03-0Relevant articles and documents

Cell-permeable small molecule probes for site-specific labeling of proteins.

Yeo, Dawn S Y,Srinivasan, Rajavel,Uttamchandani, Mahesh,Chen, Grace Y J,Zhu, Qing,Yao, Shao Q

, p. 2870 - 2871 (2007/10/03)

We have successfully synthesized a number of small molecule probes designed for site-specific labeling of N-terminal cysteine-containing proteins expressed in live cells. Their utility for site-specific, covalent modifications of proteins was successfully demonstrated with purified proteins in vitro, and with live bacterial cells in vivo.

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