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2566-32-7

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2566-32-7 Usage

Description

N-ME-DL-VAL-OH HCL, also known as N-Methyl-dl-valine hydrochloride, is an N-methylamino acid that is the N-methyl derivative of valine. It is a white powder and is a significant component in the synthesis of various pharmaceuticals and biologically active compounds.

Uses

Used in Pharmaceutical Industry:
N-ME-DL-VAL-OH HCL is used as an intermediate for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Research and Development:
N-ME-DL-VAL-OH HCL is used as a research compound for studying the properties and interactions of N-methylated amino acids. This can lead to a better understanding of their role in various biological processes and the development of novel therapeutic strategies.
Used in Chemical Synthesis:
N-ME-DL-VAL-OH HCL is used as a building block in the chemical synthesis of complex organic molecules, including those with potential applications in the fields of medicine, agriculture, and materials science.
Used in Analytical Chemistry:
N-ME-DL-VAL-OH HCL can be used as a reference compound or standard in analytical chemistry for the identification and quantification of related compounds in various samples, such as pharmaceutical formulations or biological tissues.

Check Digit Verification of cas no

The CAS Registry Mumber 2566-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2566-32:
(6*2)+(5*5)+(4*6)+(3*6)+(2*3)+(1*2)=87
87 % 10 = 7
So 2566-32-7 is a valid CAS Registry Number.

2566-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methylvaline

1.2 Other means of identification

Product number -
Other names N-ME-DL-VAL-OH HCL

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:2566-32-7 SDS

2566-32-7Upstream product

2566-32-7Relevant articles and documents

Dudawalamides A-D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens

Almaliti, Jehad,Malloy, Karla L.,Glukhov, Evgenia,Spadafora, Carmenza,Gutiérrez, Marcelino,Gerwick, William H.

, p. 1827 - 1836 (2017/06/28)

A family of 2,2-dimethyl-3-hydroxy-7-octynoic acid (Dhoya)-containing cyclic depsipeptides, named dudawalamides A-D (1-4), was isolated from a Papua New Guinean field collection of the cyanobacterium Moorea producens using bioassay-guided and spectroscopic approaches. The planar structures of dudawalamides A-D were determined by a combination of 1D and 2D NMR experiments and MS analysis, whereas the absolute configurations were determined by X-ray crystallography, modified Marfey's analysis, chiral-phase GCMS, and chiral-phase HPLC. Dudawalamides A-D possess a broad spectrum of antiparasitic activity with minimal mammalian cell cytotoxicity. Comparative analysis of the Dhoya-containing class of lipopeptides reveals intriguing structure-activity relationship features of these NRPS-PKS-derived metabolites and their derivatives.

Two new 14-membered cyclopeptide alkaloids from Zizyphus xylopyra

Pandey, Manoj B.,Singh, Sarita,Malhotra, Meenakshi,Pandey, Vidya B.,Singh, Tryambak D.

experimental part, p. 836 - 841 (2012/10/07)

The phytochemical investigation of the bark of Zizyphus xylopyra resulted in the isolation of two new 14-membered ring cyclopeptide alkaloids, xylopyrine-G and xylopyrine H. Their structures have been established by chemical and spectral evidences.

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