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1105596-98-2

C23H37BrOSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1105596-98-2 Structure

  • Basic information

    1. Product Name: C23H37BrOSi
    2. Synonyms: C23H37BrOSi
    3. CAS NO:1105596-98-2
    4. Molecular Formula:
    5. Molecular Weight: 437.536
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1105596-98-2.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: C23H37BrOSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H37BrOSi(1105596-98-2)
    11. EPA Substance Registry System: C23H37BrOSi(1105596-98-2)

  • 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: 1105596-98-2(Hazardous Substances Data)

1105596-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1105596-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,5,5,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1105596-98:
(9*1)+(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*6)+(2*9)+(1*8)=152
152 % 10 = 2
So 1105596-98-2 is a valid CAS Registry Number.

1105596-98-2Upstream product

1105596-98-2Downstream Products

1105596-98-2Relevant articles and documents

Nickel-catalyzed Negishi cross-couplings of secondary nucleophiles with secondary propargylic electrophiles at room temperature

Smith, Sean W.,Fu, Gregory C.

supporting information; experimental part, p. 9334 - 9336 (2009/05/16)

(Chemical Equation Presented) Mild thing: The first nickel-based catalysts for cross-couplings of secondary organometallic nucleophiles with secondary alkyl electrophiles have been developed. Thus, Negishi reactions proceed under mild conditions (at room temperature with no basic activators) in the presence of NiCl2·glyme and a tridentate ligand (see scheme).

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