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Merck

902489

Tris(trimethylsilyl)silanol

≥95%

동의어(들):

(Hydroxy-bis(trimethylsilyl)silyl)-trimethylsilane, (TMS)3SiOH, 1,1,1,3,3,3-Hexamethyl-2-(trimethylsilyl)trisilan-2-ol, Supersilanol

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C9H28OSi4
CAS 번호:
Molecular Weight:
264.66
UNSPSC Code:
12161700
NACRES:
NA.22
MDL number:
Assay:
≥95%
Form:
liquid
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assay

≥95%

form

liquid

reaction suitability

reaction type: C-C Bond Formation

refractive index

n/D 1.496

density

0.859 g/mL

SMILES string

[Si]([Si](C)(C)C)([Si](C)(C)C)([Si](C)(C)C)O

InChI

1S/C9H28OSi4/c1-11(2,3)14(10,12(4,5)6)13(7,8)9/h10H,1-9H3

InChI key

ABTWCNHNRLMBFR-UHFFFAOYSA-N

Application

Under a dual catalytic copper/photoredox manifold, this supersilanol has been demonstrated by the MacMillan lab to be an excellent reagent for the trifluoromethylation of alkyl halides and aryl halides to yield alkyl-CF3 and aryl-CF3 in high yields. In both cases, these reactions exhibit wide substrate scope with good functional group tolerance. More specifically, a variety of 5-membered and 6-membered heteroaryl halides can be readily converted to the corresponding trifluoromethylheteroarenes under mild conditions. To be use in conjunction with dMesSCF3 (901466) and Ir photocatalyst (902217 or 902225).


저장 등급

10 - Combustible liquids

wgk

WGK 3

flash_point_f

200.3 °F

flash_point_c

93.5 °C



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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문



Timothy J Boyle et al.
Inorganic chemistry, 57(15), 8806-8820 (2018-07-07)
In an effort to generate single-source precursors for the production of metal-siloxide (MSiO x) materials, the tris(trimethylsilyl)silanol (H-SST or H-OSi(SiMe3)3 (1) ligand was reacted with a series of group 4 and 5 metal alkoxides. The group 4 products were crystallographically
Annie J Jiang et al.
Journal of the American Chemical Society, 131(46), 16630-16631 (2009-11-19)
Mo and W MonoAryloxide-Pyrrolide (MAP) olefin metathesis catalysts can couple terminal olefins to give as high as >98% Z-products in moderate to high yields with as little as 0.2% catalyst. Results are reported for 1-hexene, 1-octene, allylbenzene, allyltrimethylsilane, methyl-10-undecenoate, methyl-9-decenoate
Chip Le et al.
Science (New York, N.Y.), 360(6392), 1010-1014 (2018-06-02)
Transition metal-catalyzed arene functionalization has been widely used for molecular synthesis over the past century. In this arena, copper catalysis has long been considered a privileged platform due to the propensity of high-valent copper to undergo reductive elimination with a



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SKUGTIN
902489-1G04061838692955
902489-5G04061838692962