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4-hydroxy-2-(2-methyl-1,3-dioxolan-2-yl)-N-(2-phenylethyl)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128746-84-9

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128746-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128746-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128746-84:
(8*1)+(7*2)+(6*8)+(5*7)+(4*4)+(3*6)+(2*8)+(1*4)=159
159 % 10 = 9
So 128746-84-9 is a valid CAS Registry Number.

128746-84-9SDS

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 4-hydroxy-2-(2-methyl-1,3-dioxolan-2-yl)-N-(2-phenylethyl)butanamide

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-(2-methyl-1,3-dioxolan-2-yl)-N-phenethylbutanamide

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:128746-84-9 SDS

128746-84-9Relevant academic research and scientific papers

REACTION OF α-ACETYLBUTYROLACTONE WITH AMINES

Malawska, Barbara,Gorczyca, Maria

, p. 63 - 68 (2007/10/02)

The reaction of α-acetylbutyrolactone and its ethylene ketal derivative with primary amines were investigated.Depending on the reaction conditions derivatives of butyrolactone (-) or urea (, ) or γ-hydroxybutyric acid (-) were obtained.The cyclisation reaction of γ-hydroxybutyric acid derivatives (-) to the corresponding 1,3-disubstituted pyrrolidinone-2 were also examined.Keywords: α-acetylbutyrolactone, γ-hydroxybutyric acid, elemental and spectral analysis, cyclization reaction

Synthesis and crystal and molecular structure of new N-substituted γ-hydroxybutyramides

Malawska, B.,Gorczyca, M.,Wieczorek, W.

, p. 139 - 144 (2007/10/02)

The N-(2-phenylethyl)amide of α-(1',1'-ethylenedioxy)-ethyl-γ-hydroxybutyric acid (II) and the N-(p-methoxybenzyl)amide of α-(1',1'-ethylenedioxy)-ethyl-γ-hydroxybutyric acid (III) have been synthesized and the crystal structure of III has been solved.Compound III, C16H23O5N, crystallizes in the monoclinic space group P21/c with a = 12.572(2), b = 11.149(2), c = 12.317(2) Angstroem and β = 106.53(1) deg.The structure was solved by direct methods, and refined by full-matrix least squares to give R = 0.040 (Rw = 0.047) for 2004 intensities.The dioxolane ringhas a deformed half-chair conformation.

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