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Silane, [1,1'-biphenyl]-4,4'-diylbis[trimethyl-], also known as bis(trimethylsilyl)biphenyl, is an organosilicon compound with the chemical formula (CH3)3Si-C6H4-C6H4-Si(CH3)3. Silane, [1,1'-biphenyl]-4,4'-diylbis[trimethyl- features a biphenyl core, which consists of two benzene rings connected by a single bond, with each benzene ring substituted by a trimethylsilyl group (-Si(CH3)3). The trimethylsilyl groups are electron-donating and can stabilize the molecule by delocalizing electrons. Bis(trimethylsilyl)biphenyl is a colorless, crystalline solid that is sensitive to air and moisture, and it is commonly used as a reagent in organic synthesis, particularly in the protection of phenolic hydroxyl groups and as a precursor for the synthesis of other organosilicon compounds.

1625-89-4

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1625-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1625-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1625-89:
(6*1)+(5*6)+(4*2)+(3*5)+(2*8)+(1*9)=84
84 % 10 = 4
So 1625-89-4 is a valid CAS Registry Number.

1625-89-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[4-(4-trimethylsilylphenyl)phenyl]silane

1.2 Other means of identification

Product number -
Other names Silane,[1,1'-biphenyl]-4,4'-diylbis[trimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1625-89-4 SDS

1625-89-4Relevant academic research and scientific papers

Nickel- and palladium-catalyzed cross-coupling reactions at the bridgehead of bicyclo[1.1.1]pentane derivatives - A convenient access to liquid crystalline compounds containing bicyclo[1.1.1]pentane moieties

Messner, Matthias,Kozhushkov, Sergei I.,De Meijere, Armin

, p. 1137 - 1155 (2007/10/03)

Radical addition reactions of organyl iodides 7a-s onto [1.1.1]propellane (2) followed by halogen-lithium exchange and transmetallation with zinc chloride, as well as additions of Grignard reagents to 2, have furnished a variety of 3-substituted bicyclo[1.1.1]pentyl-1-magnesium (14) and -zinc (19) derivatives. The latter have been coupled with various alkenyl, aryl, and biaryl halides and triflates under NiCl2dppe, Pd(PPh3)4, or PdCl2(dppf) catalysis to give a number of 1,3-disubstituted bicyclo[1.1.1]pentyl derivatives 17, 20, and 23, several of which exhibit liquid crystalline properties, in moderate to very good yields. The coupling products 20ca, 23ab, 23ae, 23ff, and 23fg have been further transformed to yield bicyclo[1.1.1]pentyl derivatives 32, 24ab, 24ae, 27ff, and 27fg, respectively, bearing alkynyl, cyano, and/or alkenyl groups.

Photochemische Untersuchungen an Bis(phenyl)(diarsan)platin(II)-Verbindungen

Brune, Hans-Albert,Klotzbuecher, Rainer,Schmidtberg, Guenther

, p. 389 - 402 (2007/10/02)

The compounds (η2-diarsane)bis(phenyl)platinum(II) with either a CH3, (CH3)2CH, (CH3)3C, F, Br, CF3, (CH3)3Si in the 4-position of the platinum-bound phenyl rings have been synthesized and studied photochemically.After excitation into the longest wavelength absorption band they eliminate the two substituted, platinum-bound rings as a biphenyl, but are photo-stable when excited by shorter wavelength UV-radiation.The elimination is exclusively intramolecular and stereospecific; it is an example of a concerted pericyclic at a transition metal.

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