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16844-98-7

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16844-98-7 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 16844-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,4 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16844-98:
(7*1)+(6*6)+(5*8)+(4*4)+(3*4)+(2*9)+(1*8)=137
137 % 10 = 7
So 16844-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O2Si/c1-5-6(7)8-9(2,3)4/h5H2,1-4H3

16844-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylsilyl propanoate

1.2 Other means of identification

Product number -
Other names Silanol,trimethyl-,propionate

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:16844-98-7 SDS

16844-98-7Relevant articles and documents

Production of acyloxysilane

-

Paragraph 0059-0064, (2021/10/30)

[A] a method for producing functional chemicals useful as efficient acyloxysilane. The silanol Si-to-OH bond [a], in the presence of a catalyst, comprising the step of reacting a carboxylic acid anhydride, Si-to-OCO bond (OCO is, oxycarbonyl groups (=O) O-a C shown. ) Having an acyloxysilane manufacturing method, wherein the catalyst, or (2) (1) production of acid catalyst selected from the next acyloxysilane. (1) 3 - 15 Of the periodic table of the first group the first group element selected from the perchlorate salt, trifluoromethanesulfonic acid salt, a bis (trifluoromethanesulfonyl imide) salt, lithium hexafluorophosphate salt, chloride, or bromide; inorganic acids; or an organic acid. (2) Inorganic or organic solid acid compounds[Drawing] no

Bimetallic reductive elimination from dinuclear Pd(III) complexes

Powers, David C.,Benitez, Diego,Tkatchouk, Ekaterina,Goddard, William A.,Ritter, Tobias

supporting information; experimental part, p. 14092 - 14103 (2011/01/09)

In 2009, we reported C-halogen reductive elimination reactions from dinuclear Pd(III) complexes and implicated dinuclear intermediates in Pd(OAc)2-catalyzed C-H oxidation chemistry. Herein, we report results of a thorough experimental and theor

A study on the haterogeneous reaction of trialkylsilyl chlorides with inorganic salts and monocarboxylates catalysed by PEG400

Du, Yun-Fei,Cao, Yu-Qing,Dai, Zhi,Chen, Bao-Hua

, p. 223 - 225 (2007/10/03)

The important and useful trialkylsilyl pseudohalides R3SiX, where X=NCS, NCO, N3 or CN and R=methyl or ethyl, and trimethylsilyl monocarboxylates, where X=RCOO, were readily prepared in high yields by nucleophilic substitution of R3SiCl with X ions provided by NaX or KX at room temperature catalysed by PEG400 and zinc iodide. The reactions of trimethylsilyl chloride with some metal oxysalts were also studied for the first time.

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