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2-[(TERT-BUTOXYCARBONYL)AMINO]-3-(3-FLUOROPHENYL)PROPANOIC ACID, also known as Boc-Phe(3-F)-OH, is a chemical compound with a molecular formula of C16H21NO5. It is a derivative of the amino acid phenylalanine, featuring a tert-butoxycarbonyl (Boc) protecting group attached to the amino group and a 3-fluorophenyl group attached to the carbon chain. Boc-Phe(3-F)-OH is a white to off-white crystalline powder that is stable under normal conditions of use and storage. It is commonly used as a building block in peptide synthesis and organic chemical reactions and is generally considered non-toxic, although proper safety precautions should be observed during handling.

87184-23-4

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87184-23-4 Usage

Uses

Used in Pharmaceutical Industry:
2-[(TERT-BUTOXYCARBONYL)AMINO]-3-(3-FLUOROPHENYL)PROPANOIC ACID is used as a building block for the synthesis of peptides and other bioactive molecules, contributing to the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, 2-[(TERT-BUTOXYCARBONYL)AMINO]-3-(3-FLUOROPHENYL)PROPANOIC ACID serves as a versatile intermediate for the synthesis of various organic compounds, facilitating the creation of complex molecules and chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 87184-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87184-23:
(7*8)+(6*7)+(5*1)+(4*8)+(3*4)+(2*2)+(1*3)=154
154 % 10 = 4
So 87184-23-4 is a valid CAS Registry Number.

87184-23-4SDS

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 Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-3-fluoro-

1.2 Other means of identification

Product number -
Other names 2-[(TERT-BUTOXYCARBONYL)AMINO]-3-(3-FLUOROPHENYL)PROPANOIC ACID

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:87184-23-4 SDS

87184-23-4Relevant academic research and scientific papers

HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis

-

, (2008/06/13)

The present invention concerns processes for preparing compounds of formula (I-H), or a prodrug, pharmaceutically active metabolite, or pharmaceutically active salt or solvate thereof, which are useful as inhibitors of the HIV protease enzyme.

Transport of antimicrobial agents using peptide carrier systems: Anticandidal activity of m-fluorophenylalanine-peptide conjugates

Kingsbury,Boehm,Mehta,Grappel

, p. 1725 - 1729 (2007/10/02)

A series of di- and tripeptides containing D- and L-m-fluorophenylalanine was prepared and tested in vitro for the ability to inhibit the growth of the yeast Candida albicans. The results demonstrate that peptides containing L-m-fluorophenylalanine inhibi

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