Home Cart Sign in  
Chemical Structure| 35692-27-4 Chemical Structure| 35692-27-4

Structure of 35692-27-4

Chemical Structure| 35692-27-4

Trimethoxy(4-methoxyphenyl)silane

CAS No.: 35692-27-4

4.5 *For Research Use Only !

Cat. No.: A475148 Purity: 93%

Change View

Size Price

US Stock

Global Stock

In Stock
100mg ł§Ë¶ÊÊ Inquiry Inquiry
250mg ł§î¶ÊÊ Inquiry Inquiry
1g łÍď¶ÊÊ Inquiry Inquiry
5g łÇËÿ¶ÊÊ Inquiry Inquiry

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • 100mg

    ł§Ë¶ÊÊ

  • 250mg

    ł§î¶ÊÊ

  • 1g

    łÍď¶ÊÊ

  • 5g

    łÇËÿ¶ÊÊ

In Stock

- +

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 35692-27-4 ]

CAS No. :35692-27-4
Formula : C10H16O4Si
M.W : 228.32
SMILES Code : COC1=CC=C([Si](OC)(OC)OC)C=C1
MDL No. :MFCD01861721
InChI Key :ZESWBFKRPIRQCD-UHFFFAOYSA-N
Pubchem ID :15532216

Safety of [ 35692-27-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P264-P302+P352-P304+P340-P305+P351+P338-P332+P313-P337+P313

Application In Synthesis of [ 35692-27-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 35692-27-4 ]

[ 35692-27-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 570-02-5 ]
  • [ 35692-27-4 ]
  • [ 108840-31-9 ]
YieldReaction ConditionsOperation in experiment
56% With palladium(II) trifluoroacetate; C30H30N4; silver fluoride; In N,N-dimethyl acetamide; at 110℃; for 2h; General procedure: To a mixture of aryl(trialkoxy)silane(0.20 mmol), AgF (76.6 mg, 0.60 mmol), Pd(TFA)2 (5.0 mg, 0.015 mmol,7.5 mol %), and ligand 1g (6.7 mg, 0.015 mmol, 7.5 mol %) in DMAc (1.0 mL)was added arylcarboxylic acid (0.40 mmol) at room temperature under an atmosphere of air. After the mixture was stirred at 100?or 110?C for 2-8 h, the mixture was diluted with ethyl acetate and water. The organic layer was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane/EtOAc = 20:1).
 

Historical Records

Technical Information

Categories