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13122-90-2

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  • China Biggest factory Supply High Quality Boc-L-Phenylalanyl-phenylalanine CAS 13122-90-2

    Cas No: 13122-90-2

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13122-90-2 Usage

General Description

Boc-Phe-Phe-OH is a chemical compound with the molecular formula C23H27NO5. It is also known as N-(tert-butoxycarbonyl)-L-phenylalanine-L-phenylalanine. Boc-Phe-Phe-OH is commonly used in peptide synthesis as a building block for creating new peptides. It is a white to off-white powder with a molecular weight of 397.46 g/mol. Boc-Phe-Phe-OH is a protected dipeptide, meaning it has a protective group (Boc) to prevent unwanted reactions during peptide synthesis. Boc-Phe-Phe-OH is widely used in research and pharmaceutical industries for the development of new drugs and peptides due to its stability and versatility in synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 13122-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13122-90:
(7*1)+(6*3)+(5*1)+(4*2)+(3*2)+(2*9)+(1*0)=62
62 % 10 = 2
So 13122-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C23H28N2O5/c1-23(2,3)30-22(29)25-18(14-16-10-6-4-7-11-16)20(26)24-19(21(27)28)15-17-12-8-5-9-13-17/h4-13,18-19H,14-15H2,1-3H3,(H,24,26)(H,25,29)(H,27,28)

13122-90-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H63788)  N-Boc-L-phenylalanyl-L-phenylalanine, 95%   

  • 13122-90-2

  • 1g

  • 1030.0CNY

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  • Alfa Aesar

  • (H63788)  N-Boc-L-phenylalanyl-L-phenylalanine, 95%   

  • 13122-90-2

  • 5g

  • 3859.0CNY

  • Detail

13122-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Phe-Phe-OH

1.2 Other means of identification

Product number -
Other names Boc-L-Phenylalanyl-phenylalanine

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:13122-90-2 SDS

13122-90-2Relevant articles and documents

A Comprehensive Landscape for Fibril Association Behaviors Encoded Synergistically by Saccharides and Peptides

Liu, Rongying,Zhang, Ran,Li, Long,Kochovski, Zdravko,Yao, Lintong,Nieh, Mu-Ping,Lu, Yan,Shi, Tongfei,Chen, Guosong

, p. 6622 - 6633 (2021/05/29)

Nature provides us a panorama of fibrils with tremendous structural polymorphism from molecular building blocks to hierarchical association behaviors. Despite recent achievements in creating artificial systems with individual building blocks through self-

A catalytic one-step synthesis of peptide thioacids: the synthesis of leuprorelin via iterative peptide-fragment coupling reactions

Matsumoto, Takuya,Sasamoto, Koki,Hirano, Ryo,Oisaki, Kounosuke,Kanai, Motomu

supporting information, p. 12222 - 12225 (2018/12/01)

A catalytic one-step synthesis of peptide thioacids was developed. The oxygen-sulfur atom exchange reaction converted the carboxy group at the C-terminus of the peptides into a thiocarboxy group with suppressed epimerization. This method was successfully applied to the synthesis of the peptide drug leuprorelin via an iterative fragment-coupling protocol.

On the Role of Chirality in Guiding the Self-Assembly of Peptides

Basak, Shibaji,Singh, Ishwar,Ferranco, Annaleizle,Syed, Jebreil,Kraatz, Heinz-Bernhard

, p. 13288 - 13292 (2017/10/07)

Homochirality in peptides is crucial in sustaining “like–like” intermolecular interactions that allow the formation of assemblies and aggregates and is ultimately responsible for the resulting material properties. With the help of a series of stereoisomer

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