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Acetic acid, (acetyloxy)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30379-73-8

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30379-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30379-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30379-73:
(7*3)+(6*0)+(5*3)+(4*7)+(3*9)+(2*7)+(1*3)=108
108 % 10 = 8
So 30379-73-8 is a valid CAS Registry Number.

30379-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl acetoxyacetate

1.2 Other means of identification

Product number -
Other names O-Acetylglykolsaeure-benzylester

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:30379-73-8 SDS

30379-73-8Downstream Products

30379-73-8Relevant academic research and scientific papers

Silver acetate mediated acetoxylations of alkyl halides

Nolla-Saltiel, Roberto,Carrillo-Arcos, Ulises Alonso,Porcel, Susana

supporting information, p. 165 - 169 (2014/03/21)

Silver acetate promotes the acetoxylation of alkyl halides under neutral reaction conditions. The reaction is applicable to primary and activated secondary alkyl halides, and 2,2-dibromoacetophenones for preparing the corresponding acetates in good yields. The presence of ester, amide, nitrile, hydroxy, and OTBDMS functions on the substrate is tolerated.

Hydrogen-bond-mediated folding in depsipeptide models of β-turns and α-helical turns

Gallo, Elizabeth A.,Gellman, Samuel H.

, p. 9774 - 9788 (2007/10/02)

The folding of several depsipeptides constructed from α-amino acids [L-proline (P) and L-alanine (A)] and α-hydroxy acids [L-lactic acid (L) and glycolic acid (G)] has been examined in methylene chloride solution by variable- temperature IR spectroscopy. Additional studies have been conducted in some cases, involving variable-temperature 1H NMR spectroscopy and molecular mechanics calculations. The depsipeptides include three-residue molecules (PLL, ALL, and PLG) that can form a 13-membered-ring amide-to-amide hydrogen bond, which, for a peptide backbone, would correspond to a single turn of an α-helix. These depsipeptides can also form 10-membered-ring amide-to-ester hydrogen bonds, which would correspond to β-trun formation for a peptide backbone. For PLL and PLG, distinct N-H stretch bands can be identified for three folding patterns: non-hydrogen-bonded, β-turn, and α-helical turn. IR-based van't Hoff analyses for PLL indicate that the α-helical turn and the β-turn are both modestly enthalpically favored relative to the non-hydrogen-bonded state, but neither turn is enthalpically preferred over the other. For PLG, in contrast, the α-helical turn appears to be enthalpically preferred over both of the alternative folding patterns. Comparison between PLL and ALL indicates that the N-terminal proline residue favors α-helical turn formation. The strengths of amide-to-amide and amide-to-ester hydrogen bonds have been compared in the context of a β-turn geometry by analyzing LG and AG in CH2Cl2. The amide-to-amide hydrogen bond is enthalpically favored by ca. 1.6 kcal/mol, but formation of this enthalpically stronger intramolecular hydrogen bond is more costly entropically. Extrapolation from the behavior of these depsipeptides leads us to predict that for tripeptides in a nonpolar environment, a β-turn will generally be enthalpically preferred over an isolated α-helical turn. β-Turn folding has previously been widely studied in model peptides and depsipeptides; however, the present report appears to represent the first experimental effort to model formation of a single α-helical turn.

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