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15893-47-7

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15893-47-7 Usage

General Description

H-D-LEU-NH2 is a chemical compound consisting of the amino acid leucine, which is a hydrophobic, aliphatic amino acid with a branched side chain. It is often found in proteins and is important for protein synthesis and muscle repair and growth. The H- at the beginning of the compound signifies that this is a peptide with a free amine group at the N-terminus, and the NH2 at the end signifies a free carboxylic acid group at the C-terminus. H-D-LEU-NH2 is commonly used in research and pharmaceuticals for its role in protein structure and function.

Check Digit Verification of cas no

The CAS Registry Mumber 15893-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,9 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15893-47:
(7*1)+(6*5)+(5*8)+(4*9)+(3*3)+(2*4)+(1*7)=137
137 % 10 = 7
So 15893-47-7 is a valid CAS Registry Number.

15893-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-Amino-4-methylpentanamide

1.2 Other means of identification

Product number -
Other names (2R)-2-amino-4-methylpentanamide

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:15893-47-7 SDS

15893-47-7Relevant articles and documents

Enzymatic stability of myostatin inhibitory 16-mer peptides

Hayashi, Yoshio,Odagiri, Miki,Taguchi, Akihiro,Takayama, Kentaro,Taniguchi, Atsuhiko

, p. 512 - 515 (2020/07/21)

-

Bianthryl-based organocatalysts for the asymmetric Henry reaction of fluoroketones

Otevrel, Jan,Svestka, David,Bobal, Pavel

supporting information, p. 5244 - 5248 (2019/06/07)

We have developed a catalytic system based on bianthrylbis(thiourea) for the asymmetric Henry reaction of fluoroketones and nitroalkanes that resulted from the screening of a library containing 31 chiral non-racemic organocatalysts. The corresponding adducts were isolated in up to 6 times shorter reaction time in comparison with the previously published organocatalysts. High levels of stereocontrol have been generally observed, with measured product enantiomeric excesses up to 97% and diastereomeric ratio 3:2 (anti/syn). The above-mentioned catalysts have been successfully applied to the total asymmetric synthesis of CF3-tethered (S)-halostachines, which has proved that this method constitutes an easy entry to similar enantiopure compounds.

3, 5-disubstituted hydantoin compound as well as preparation method and application thereof

-

Paragraph 0041; 0051; 0052; 0063; 0064, (2018/10/19)

The invention provides a 3, 5-disubstituted hydantoin compound as well as a preparation method and an application thereof. The structure of the compound is shown in formula I in the description. The application of the 3, 5-disubstituted hydantoin compound shown in the formula I or solvates, hydrates or salts of the compound in preparation of medicines for treating Alzheimer's disease, vascular dementia and other dementia diseases with memory impairment also belongs to the protection scope. Animal experiments prove that the compound has the effect of saving memory of animal models, has high safety, does not have mutagenicity, can stay in blood for several hours after oral administration and intravenous injection, and can enter the brain.

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