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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 161006-18-4 Chemical Structure| 161006-18-4

Structure of 161006-18-4

Chemical Structure| 161006-18-4
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Product Details of [ 161006-18-4 ]

CAS No. :161006-18-4
Formula : C12H20O2Si
M.W : 224.37
SMILES Code : OC1=CC=CC(O[Si](C)(C(C)(C)C)C)=C1
MDL No. :MFCD27945625
InChI Key :WNTUMICETVLAST-UHFFFAOYSA-N
Pubchem ID :11447440

Safety of [ 161006-18-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H318
Precautionary Statements:P280-P305+P351+P338+P310
Class:8
UN#:1760
Packing Group:

Application In Synthesis of [ 161006-18-4 ]

* 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 [ 161006-18-4 ]

[ 161006-18-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56012-38-5 ]
  • [ 161006-18-4 ]
  • C17H25NO2SSi [ No CAS ]
YieldReaction ConditionsOperation in experiment
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20℃; for 18h; Step 2: Intermediate 15-b To a solution of intermediate 15-a (7.75 g, 34.5 mmol) and intermediate 11- a (4.25 g, 32.9 mmol), in THF (33 ml_), were sequentially added triphenylphosphine (10.35 g, 39.5 mmol) and DIAD (7.68 ml, 39.5 mmol) drop wise at room temperature. The reaction was then stirred for 18 hours. Volatiles were removed in vacuo. Purification by silica gel chromatography provided intermediate 15-b as a colorless oil.
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20℃; for 18h; Step 2: Intermediate 15-b [0132] To a solution of intermediate 15-a (7.75 g, 34.5 mmol) and intermediate 11-a (4.25 g, 32.9 mmol), in THF (33 mL), were sequentially added triphenylphosphine (10.35 g, 39.5 mmol) and DIAD (7.68 ml, 39.5 mmol) drop wise at room temperature. The reaction was then stirred for 18 hours. Volatiles were removed in vacuo. Purification by silica gel chromatography provided intermediate 15-b as a colorless oil.
 

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