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[ CAS No. 1078-97-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 1078-97-3
Chemical Structure| 1078-97-3
Structure of 1078-97-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1078-97-3 ]

CAS No. :1078-97-3 MDL No. :MFCD00039299
Formula : C10H16Cl2Si2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 263.31 Pubchem ID :-
Synonyms :

Safety of [ 1078-97-3 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1078-97-3 ]

* 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 [ 1078-97-3 ]

[ 1078-97-3 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 106-37-6 ]
  • [ 75-78-5 ]
  • [ 18236-77-6 ]
  • [ 1078-97-3 ]
YieldReaction ConditionsOperation in experiment
30% Stage #1: 1.4-dibromobenzene With magnesium In tetrahydrofuran Stage #2: dimethylsilicon dichloride In tetrahydrofuran at 0℃; for 1h;
  • 3
  • [ 1078-97-3 ]
  • [ 2754-32-7 ]
YieldReaction ConditionsOperation in experiment
With NaOH In sodium hydroxide; diethyl ether aq. NaOH; (CH3)2ClSiC6H4SiCl(CH3)2 and equival. amt. of aq. NaOH in ether at about 0°C;; crystn. from ether or by addn. of C6H6 to the ether soln.;;
With sodium hydroxide In sodium hydroxide; diethyl ether (CH3)2ClSiC6H4SiCl(CH3)2 and equival. amt. of aq. NaOH in ether at about 0°C;; crystn. from ether or by addn. of C6H6 to the ether soln.;;
  • 4
  • [ 1078-97-3 ]
  • [ 1826-67-1 ]
  • [ 4519-17-9 ]
YieldReaction ConditionsOperation in experiment
79.9% In tetrahydrofuran; at -30 - 20℃;Glovebox; 1,4-Bis(chlorodimethylsilyl)benzene (4.804 g, 18.24 mmol) in THF (40 mL) is cooled in a glovebox freezer (-30 C). A solution of vinylmagnesium bromide (40.14 mmol, 40.14 mL of 1.0 M in THF) is then added slowly. This mixture is allowed to stir to room temperature overnight, and the intended reaction (see non- limiting Reaction Scheme 8) proceeds. After the reaction period, the volatiles are removed and the residue extracted and filtered using benzene. Removal of the benzene from the filtrate results in the isolation of a free flowing liquid as well as further precipitated salts. This material is filtered through a celite bed using hexane as the eluent. Removal of the volatiles results in the isolation of the desired product as a clear pale yellow liquid (3.5948 g, 79.9 %). NMR (500 MHz, Benzene-d6) d 7.51 (s, 4H), 6.30 - 6.19 (m, 1H), 5.99 - 5.91 (m, 1H), 5.69 (dd, J = 20.3, 3.8 Hz, 1H), 0.27 (s, 12H). 13C NMR (126 MHz, Benzene-d6) d 138.86, 137.74, 133.24, 132.59, -3.23.
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