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913626-19-4

3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 913626-19-4 Structure

  • Basic information

    1. Product Name: 3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile
    2. Synonyms: 3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile
    3. CAS NO:913626-19-4
    4. Molecular Formula:
    5. Molecular Weight: 280.164
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 913626-19-4.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: 3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile(913626-19-4)
    11. EPA Substance Registry System: 3-[(1S)-1-(4-bromo-phenyl)-but-3-enyloxy]-propionitrile(913626-19-4)

  • 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: 913626-19-4(Hazardous Substances Data)

913626-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913626-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,6,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 913626-19:
(8*9)+(7*1)+(6*3)+(5*6)+(4*2)+(3*6)+(2*1)+(1*9)=164
164 % 10 = 4
So 913626-19-4 is a valid CAS Registry Number.

913626-19-4Relevant articles and documents

Synthesis and PKC binding of a new class of A-ring diversifiable bryostatin analogues utilizing a double asymmetric hydrogenation and cross-coupling strategy

Wender, Paul A.,Horan, Joshua C.

, p. 4581 - 4584 (2006)

The design, asymmetric synthesis, and biological evaluation of a new class of bryostatin analogues based on a pseudosymmetric spacer domain are described. An aryl bromide diversification site is incorporated allowing access to systematically varied analog

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