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Methyl 5-(diMethylaMino)-5-oxopentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14471-87-5

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14471-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14471-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,7 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14471-87:
(7*1)+(6*4)+(5*4)+(4*7)+(3*1)+(2*8)+(1*7)=105
105 % 10 = 5
So 14471-87-5 is a valid CAS Registry Number.

14471-87-5SDS

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 methyl 5-(dimethylamino)-5-oxopentanoate

1.2 Other means of identification

Product number -
Other names N,N-Dimethylglutaramid-methylester

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:14471-87-5 SDS

14471-87-5Downstream Products

14471-87-5Relevant academic research and scientific papers

ESTERAMIDE SOLVENTS/COALESCING AGENTS IN PHYTOSANITARY, CLEANING, DEGREASING, STRIPPING, LUBRICATING, COATING, AND PIGMENT/INK COMPOSITIONS

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Page/Page column 18, (2011/07/29)

Esteramide compounds are useful solvents/coalescing agents for a variety of phytosanitary, cleaning, degreasing, stripping, lubricating, coating and pigment/ink compositions.

Conformation of Nα-substituted hydrazino acetamides in CDCl3, the precious help of the analysis of Δδ between amidic hydrogens, and correlation to the conformation of aza-β3- peptides

Salauen, Arnaud,Favre, Annaick,Le Grel, Barbara,Potel, Michel,Le Grel, Philippe

, p. 150 - 158 (2007/10/03)

We studied the conformation of a series of primary amides in a solution of chloroform. Classical NMR tools such as dilution experiments, influence of DMSO, and 2D-NOESY, together with X-ray diffraction, were combined with an analysis of the difference of the chemical shift Δδ between the geminal amidic protons. This study was addressed in order to understand the conformation adopted by hydrazino acetamides 1a and 1b as model compounds for aza-β3-peptides. In this manner, it was possible to show that the amidic group of these compounds acts as a H-bond donor and interacts with two different H-bond acceptors. We concluded that the hydrazinoturn, a specific bifurcated H-bond system observed in the solid state, is also the preferred conformation of hydrazino acetamides 1a and 1b in solution. Our results show that the short-range interaction with the Nα-nitrogen lone pair not only stabilizes the C8 pseudocycle but could also contribute to the folding process of aza-β3-peptides. In light of this, it could explain why aza-β3-peptides develop a different H-bond network in comparison to their isosteric β3-peptides analogues. Our work is in keeping with the recent interest of hydrazino peptides as an extension of the β-peptide concept.

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