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111819-71-7

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111819-71-7 Usage

General Description

(R)-2-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde is a chemical compound that belongs to the class of aldehydes. It is commonly used as a fragrance ingredient in various personal care and household products due to its pleasant odor. The compound is also used as a flavoring agent in food products. It is a clear, colorless liquid with a molecular formula of C11H24O2Si and a molecular weight of 216.40 g/mol. The chemical is synthesized through the addition of a propionaldehyde group to a tert-butyl-dimethyl-silanyloxy group, leading to the formation of (R)-2-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde. It should be handled with care and stored in a cool, dry place.

Check Digit Verification of cas no

The CAS Registry Mumber 111819-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111819-71:
(8*1)+(7*1)+(6*1)+(5*8)+(4*1)+(3*9)+(2*7)+(1*1)=107
107 % 10 = 7
So 111819-71-7 is a valid CAS Registry Number.

111819-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-[tert-butyl(dimethyl)silyl]oxypropanal

1.2 Other means of identification

Product number -
Other names Propanal,2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-,(R)

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:111819-71-7 SDS

111819-71-7Downstream Products

111819-71-7Relevant articles and documents

Structure–activity relationship study of the anti-obesity natural product yoshinone A

Kawazoe, Yoshinori,Itakura, Yuki,Inuzuka, Toshiyasu,Omura, Sachikazu,Uemura, Daisuke

, p. 226 - 232 (2021/03/06)

Yoshinone A was derived from marine algae and shown to inhibit adipogenic differentiation. The natural compound is composed of a γ-pyrone ring and a side chain and that contains two asymmetric carbons. Although their absolute configuration has been determ

Rapid de Novo Preparation of 2,6-Dideoxy Sugar Libraries through Gold-Catalyzed Homopropargyl Orthoester Cyclization

Yalamanchili, Subbarao,Miller, William,Chen, Xizhao,Bennett, Clay S.

supporting information, p. 9646 - 9651 (2019/12/02)

A flexible de novo route capable of producing libraries of 2,6-dideoxy sugars is described. We have found that Au(JackiePhos)SbF6MeCN promotes the conversion of homopropargyl orthoesters into functionalized 2,3-dihydro-4H-pyran-4-ones in good t

Stereoselective Access to (E)-1,3-Enynes through Pd/Cu-Catalyzed Alkyne Hydrocarbation of Allenes

Jeanne-Julien, Louis,Masson, Guillaume,Kouoi, Remy,Regazzetti, Anne,Genta-Jouve, Grégory,Gandon, Vincent,Roulland, Emmanuel

supporting information, (2019/05/08)

PdII and CuI cooperate in catalyzing the alkynes hydrocarbation of allenes (AHA) giving (E)-1,3-enynes with high yields, atom economy, and high regio-/stereoselectivities. We devised new efficient conditions and expanded the substrat

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