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4-Pentenoic acid, trimethylsilyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23523-56-0

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23523-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23523-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,2 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23523-56:
(7*2)+(6*3)+(5*5)+(4*2)+(3*3)+(2*5)+(1*6)=90
90 % 10 = 0
So 23523-56-0 is a valid CAS Registry Number.

23523-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylsilyl pent-4-enoate

1.2 Other means of identification

Product number -
Other names 4-pentenoyloxytrimethylsilane

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:23523-56-0 SDS

23523-56-0Relevant academic research and scientific papers

The nematic discotic phase in materials containing a siloxane core

Kouwer, Paul H. J.,Jager, Walter F.,Mijs, Wim J.,Picken, Stephen J.,Shepperson, Keith J.,Mehl, Georg H.

, p. 377/[1419]-385/[1427] (2004)

The synthesis of a series of novel multipodes based on disc-shaped mesogens with a siloxane core is described. Their phase behaviour is characterised, and compared to the liquid crystalline properties of the discotic molecules without the siloxane moietie

One-pot synthesis of 3-hydroxymaleic anhydrides by cyclization of 1,1-bis(trimethylsilyloxy)ketene acetals with oxalyl chloride

Rotzoll, Sven,Ullah, Ehsan,G?rls, Helmar,Fischer, Christine,Langer, Peter

, p. 2647 - 2656 (2007/10/03)

Functionalized 3-hydroxymaleic anhydrides were prepared by cyclization of 1,1-bis(trimethylsilyloxy)ketene acetals with oxalyl chloride.

Compound having silsesquioxane skeleton and its polymer

-

Page 32, (2010/02/10)

The present invention relates to a compound represented by Formula (1) and a polymer obtained using the compound: wherein R1 is phenyl which may have substituents, Q1 is hydrogen, halogen, alkyl having 1 to 10 carbon atoms, cycloprop

Carbon kinetic isotope effects and transition structures in the rearrangements of allyl vinyl ethers. 2-(trimethylsiloxy)- and 2-(methoxycarbonyl)-3-oxa-1,5-hexadiene

Kupczyk-Subotkowska, Lidia,Saunders Jr., William H.,Shine, Henry J.,Subotkowski, Witold

, p. 7088 - 7093 (2007/10/02)

14C KIE (kinetic isotope effects) were measured for the C-1, C-2, C-4, and C-6 positions in the rearrangement of 2-(trimethylsiloxy)- (1a) and 2-(methoxycarbonyl)-3-oxa-1,5-hexadiene (1b). The data, along with earlier C-4 and C-6 deuterium KIE, were fitted to Bebovib modeling calculations. The calculations show that in the transition structure (TS) for 1a 70-80% bond breaking and 20% of bond making occurs, whereas in the TS of 1b both bond breaking and bond making amount to 30-40%. Results for 1a and 1b are compared with earlier results for the parent compound, allyl vinyl ether.

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