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N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester is a protected amino acid pair that plays a crucial role in the synthesis of polypeptides. N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester is designed to facilitate the formation of peptide bonds between L-alanine and L-glutamic acid, while the bis(1,1-dimethylethyl) ester groups protect the carboxylic acid functionality, allowing for controlled and efficient peptide synthesis.

45272-19-3

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45272-19-3 Usage

Uses

Used in Pharmaceutical Industry:
N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester is used as a building block in the synthesis of polypeptides for various pharmaceutical applications. Its protected structure ensures that the amino acids are incorporated into the desired peptide sequence without unwanted side reactions, leading to the production of high-quality and therapeutically relevant polypeptides.
Used in Research and Development:
In the field of research and development, N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester serves as an essential component in the design and synthesis of novel polypeptides with potential biological activities. Its protected nature allows researchers to explore new peptide sequences and investigate their properties, paving the way for the discovery of new therapeutic agents and diagnostic tools.
Used in Cosmetic Industry:
N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester is also utilized in the cosmetic industry for the development of polypeptide-based skincare products. The protected amino acid pair can be incorporated into cosmetic formulations to provide targeted benefits, such as anti-aging, skin repair, and moisturization, by modulating the skin's natural peptide signaling pathways.
Overall, N-L-Alanyl-L-glutaMic Acid Bis(1,1-diMethylethyl) Ester is a versatile and valuable compound in various industries, particularly in the synthesis of polypeptides for pharmaceutical, research, and cosmetic applications. Its protected structure ensures efficient and controlled peptide synthesis, leading to the development of innovative and effective products.

Check Digit Verification of cas no

The CAS Registry Mumber 45272-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,2,7 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 45272-19:
(7*4)+(6*5)+(5*2)+(4*7)+(3*2)+(2*1)+(1*9)=113
113 % 10 = 3
So 45272-19-3 is a valid CAS Registry Number.

45272-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ditert-butyl (2S)-2-[[(2S)-2-aminopropanoyl]amino]pentanedioate

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:45272-19-3 SDS

45272-19-3Downstream Products

45272-19-3Relevant academic research and scientific papers

CANNABINOID PRODRUG COMPOUNDS

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Paragraph 0019, (2021/04/02)

A prodrug compound of cannabidiol (CBD), pharmaceutical composition thereof and methods of use thereof in patients in need.

METHODS AND COMPOSITIONS FOR TREATING CANCER

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Page/Page column 26, (2019/02/15)

Methods for treating cancer are disclosed which comprise administering to a subject T cells which have been pretreated ex vivo or in vitro with fenofibric acid (FFA), an FFA prodrug, or a derivative thereof that has PPAR-α agonist activity. These compound

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