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tert-butyl 2-(trimethylsilyl)phenyl ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162052-57-5

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162052-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162052-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,5 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162052-57:
(8*1)+(7*6)+(6*2)+(5*0)+(4*5)+(3*2)+(2*5)+(1*7)=105
105 % 10 = 5
So 162052-57-5 is a valid CAS Registry Number.

162052-57-5Downstream Products

162052-57-5Relevant academic research and scientific papers

Silyl migration in the photochemical reactions of 2- trimethylsilylmethylphenyl ketones

Saito, Masaichi,Saito, Akitomo,Ishikawa, Yuko,Yoshioka, Michikazu

, p. 3139 - 3141 (2005)

(Chemical Equation Presented) Irradiation of 2-trimethylsilylmethylphenyl ketones 1 gives benzocyclobutenols 2 and 5 together with siloxybenzocyclobutenes 4. Compound 4 arises from the novel photoinduced 1,5-silyl migration of 1. Irradiation of 1 in the p

Formation of Benzocyclobuten-1-ol Derivatives by Intramolecular Cylization of o-Acylbenzyllithiums

Kobayashi, Kazuhiro,Kawakita, Masataka,Mannami, Tohru,Konishi, Hisatoshi

, p. 733 - 736 (1995)

Reaction between the carbanions, generated in situ by the treatment of o-(trimethylsilylmethyl)phenyl ketones with lithium diisopropylamide (LDA), and chlorotrimethylsilane affords the corresponding 1-(trimethylsilyloxy)-2-trimethylsilybenzocyclobutene de

Ruthenium-catalyzed carbon-carbon bond formation via the cleavage of an unreactive aryl carbon-nitrogen bond in aniline derivatives with organoboronates

Ueno, Satoshi,Chatani, Naoto,Kakiuchi, Fumitoshi

, p. 6098 - 6099 (2008/02/08)

The RuH2(CO)(PPh3)3-catalyzed reaction of 2-amino-6-methylacetophenone with phenylboronic acid 2,2-dimethyl-1,3-propanediol ester in refluxing toluene gave the corresponding phenylation product in 83% yield via aryl carbon

Intramolecular Cyclizations of o-Acylbenzyllithiums. Formation of Benzocyclobuten-1-ol Derivatives and Their Thermal Isomerization

Kobayashi, Kazuhiro,Kawakita, Masataka,Uchida, Masaharu,Nishimura, Koichi,Mannami, Tohru,Irisawa, Susumu,Morikawa, Osamu,Konishi, Hisatoshi

, p. 3557 - 3562 (2007/10/03)

The formation of benzocyclobutenol derivatives by intramolecular cyclizations of o-acylbenzyllithiums is described. Treatment of o-(trialkylsilylmethyl)phenyl ketones with lithium diisopropylamide (LDA) followed by quenching of the resulting benzylic carb

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