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Home > Encyclopedia > 4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID structure

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID 

structure
  • CAS No:

    159191-56-7

  • Formula:

    C12H21BO3Si

  • Chemical Name:

    4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID

  • Synonyms:

    oxy)phenyL;4-(T-BUTYL DIMETHYLSILOXY) PHENYL BORONIC ACID;4-(TERT-BUTYL DIMETHYLSILOXY)PHENYL BORONIC ACID;4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID;4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORONIC ACID;AKOS BRN-0412;4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORON;4-(tert-Butyldimethylsilyloxy)benzeneboronic acid

  • Categories:

    Organic Chemistry  >  Coordination Complexes

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID Basic Attributes

252.19

252.1353012

DTXSID90455505

Characteristics

1.01±0.1 g/cm3

194-198 °C (lit.)

321.4±44.0 °C(Predicted)

8.68±0.16

Safety Information

3

Xi

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONICACID Use and Manufacturing

Reactant involved in:• ;Asymmetric addition reactions with β-substituted cyclic enones1• ;Hydroarylation and heterocyclization with phenylpropiolates2• ;Double Suzuki-Miyaura coupling reactions3Starting material for the synthesis of red electroluminescent polyfluorenes4Reactant involved in the synthesis of biologically active molecules including:• ;Phenylpyridone derivatives as MCH1R antagonists5• ;Atromentin and its O-alkylated derivatives3• ;Gelatinases and MT1-MMP inhibitors6

Computed Properties

Molecular Weight:252.19
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:252.1353012
Monoisotopic Mass:252.1353012
Topological Polar Surface Area:49.7
Heavy Atom Count:17
Complexity:243
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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