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  • 1583286-76-3 Structure
  • Basic information

    1. Product Name: C15H22BNO3
    2. Synonyms:
    3. CAS NO:1583286-76-3
    4. Molecular Formula:
    5. Molecular Weight: 275.156
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1583286-76-3.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: C15H22BNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H22BNO3(1583286-76-3)
    11. EPA Substance Registry System: C15H22BNO3(1583286-76-3)
  • 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: 1583286-76-3(Hazardous Substances Data)

1583286-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1583286-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,3,2,8 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1583286-76:
(9*1)+(8*5)+(7*8)+(6*3)+(5*2)+(4*8)+(3*6)+(2*7)+(1*6)=203
203 % 10 = 3
So 1583286-76-3 is a valid CAS Registry Number.

1583286-76-3Downstream Products

1583286-76-3Relevant articles and documents

Rhodium-catalyzed intermolecular C-H silylation of arenes with high steric regiocontrol

Chen, Cheng,Hartwig, John F.

, p. 853 - 857 (2014/03/21)

Regioselective C-H functionalization of arenes has widespread applications in synthetic chemistry. The regioselectivity of these reactions is often controlled by directing groups or steric hindrance ortho to a potential reaction site. Here, we report a catalytic intermolecular C-H silylation of unactivated arenes that manifests very high regioselectivity through steric effects of substituents meta to a potential site of reactivity. The silyl moiety can be further functionalized under mild conditions but is also inert toward many common organic transformations, rendering the silylarene products useful building blocks. The remote steric effect that we observe results from the steric properties of both the rhodium catalyst and the silane.

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