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4818-06-8

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4818-06-8 Usage

General Description

Z-ILE-PHE-OME is a chemical compound consisting of three amino acids - isoleucine, phenylalanine, and ornithine. These amino acids play important roles in various biological processes in the body. Isoleucine is an essential amino acid that is involved in protein synthesis and regulation of blood sugar levels. Phenylalanine is also an essential amino acid that is a precursor to various important molecules in the body, such as tyrosine and neurotransmitters. Ornithine is a non-protein amino acid that is involved in the urea cycle, which helps to remove ammonia from the body. Z-ILE-PHE-OME may have potential therapeutic applications due to the combination of these amino acids and their individual benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 4818-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4818-06:
(6*4)+(5*8)+(4*1)+(3*8)+(2*0)+(1*6)=98
98 % 10 = 8
So 4818-06-8 is a valid CAS Registry Number.

4818-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-Ile-Phe-OMe

1.2 Other means of identification

Product number -
Other names -

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:4818-06-8 SDS

4818-06-8Upstream product

4818-06-8Downstream Products

4818-06-8Relevant articles and documents

Formation and isolation of simple, stable, acyclic di- and tripeptide hemiacetals

Miller, John F.,Spaltenstein, Andrew

, p. 2521 - 2524 (2007/10/03)

Di- and tripeptide aldehydes were found to undergo reaction with methanol to afford the corresponding methyl hemiacetals. These compounds, which possessed unusual stability, were isolated and characterized using NMR techniques and a chemical correlation experiment.

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