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ETHYL ACETATE-D3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90691-33-1

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90691-33-1 Usage

Uses

ETHYL ACETATE-D3 is used as a solvent in organic reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 90691-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90691-33:
(7*9)+(6*0)+(5*6)+(4*9)+(3*1)+(2*3)+(1*3)=141
141 % 10 = 1
So 90691-33-1 is a valid CAS Registry Number.

90691-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL ACETATE-D3

1.2 Other means of identification

Product number -
Other names Aethyl-trideuteroacetat

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:90691-33-1 SDS

90691-33-1Downstream Products

90691-33-1Relevant academic research and scientific papers

A Bidentate Ru(II)-NC Complex as a Catalyst for Semihydrogenation of Alkynes to (E)-Alkenes with Ethanol

Chen, Dafa,Gong, Dawei,Hu, Bowen,Kong, Degong,Xia, Haiping,Yang, Weiwei

, (2020/03/19)

Four Ru(II)-NC complexes were tested as catalysts for semihydrogenation of internal alkynes to (E)-alkenes with ethanol, and the complex {(C5H4N)(C6H4)}RuCl(CO)(PPh3)2 (1a) showed the highest activity. The reactions proceeded well with 1 mol % catalyst loading and 0.1 equiv of t-BuONa at 110 °C for 1 h, and 32 alkenes were synthesized with excellent E:Z selectivity. This is the first ruthenium-catalyzed semihydrogenation of internal alkynes to (E)-alkenes using ethanol as the hydrogen donor.

VIBRATIONAL SPECTRA, NORMAL VIBRATIONS AND ROTATIONAL ISOMERISM OF ETHYL ACETATE AND THREE DEUTERATED ANALOGUES

Mido, Yoshiyuki,Shiomi, Hidenori,Matsuura, Hiroatsu,Raso, Miguel Angel,Garcia, M. Victoria,Morcillo, Jesus

, p. 253 - 278 (2007/10/02)

IR and Raman spectra of ethyl acetates, CH3COOC2H5, CD3COOC2H5, CH3COOC2D5 and CD3COOC2D5 in the liquid and crystalline states have been recorded in the 3500-200 cm-1 region.These spectra are analysed on the basis of spectral comparison both among themselves and with spectra of the trichloro analogues CCl3COOC2H5 and CCl3COOC2D5 previously studied.All the ethyl acetates in the crystalline state give two completely separated carbonyl stretching Raman bands, suggesting that two, or an even number of molecules, exist in the crystal unit.Liquid-state spectra exhibit many band pairs arising from the trans-trans and trans-gauche conformers around CX3CO-O-CX2CX3 axes (X=H and D) and the bands of the trans-trans conformer persist in the crystalline state.Normal coordinate calculations for the four species have been carried out on the two isomeric models using an MVIB program.The results explain wavenumber shifts on deuteration and the nature and separation of band pairs satisfactorily, and suggest that a large amount of vibrational coupling exists among skeletal stretching vibrations.

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