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Z-PRO-HYP-OH, also known as Z-protected proline hydroxyproline, is a synthetic peptide derivative that plays a significant role in the field of biochemistry and pharmaceuticals. Z-PRO-HYP-OH is characterized by its unique structure, which includes a proline residue connected to a hydroxyproline residue, both of which are essential amino acids. The "Z" in its name stands for the benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. Z-PRO-HYP-OH is crucial for the formation of collagen, a major structural protein in the human body, and has potential applications in the development of therapeutics for connective tissue disorders and other related conditions.

55878-58-5

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55878-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55878-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,7 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55878-58:
(7*5)+(6*5)+(5*8)+(4*7)+(3*8)+(2*5)+(1*8)=175
175 % 10 = 5
So 55878-58-5 is a valid CAS Registry Number.

55878-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4R)-4-hydroxy-1-[(2S)-1-phenylmethoxycarbonylpyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid

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

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More Details:55878-58-5 SDS

55878-58-5Relevant academic research and scientific papers

Synthesis of fmoc-pro-hyp(TBDPS)-gly-OH and its application as a versatile building block for the preparation of collagen model peptides

Erdmann, Roman S.,Wennemers, Helma

experimental part, p. 143 - 147 (2009/06/19)

The efficient synthesis of the tripeptidic building block Fmoc-Pro-Hyp(TBDPS)-Gly-OH and its application for the preparation of collagen model peptides (CMPs) has been achieved. The silyl ether protecting group prevents undesired side reactions during the

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