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FMOC-PHE(3-I)-OH, with the molecular formula C29H23NO4 and a molecular weight of 449.49 g/mol, is a phenylalanine derivative featuring a 3-iodo substitution on the phenyl ring. This solid compound is soluble in organic solvents like dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), and is typically supplied as a crystalline powder. It plays a significant role in organic synthesis and peptide chemistry, serving as a building block for the assembly of peptides and proteins.

210282-31-8

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210282-31-8 Usage

Uses

Used in Organic Synthesis:
FMOC-PHE(3-I)-OH is used as a building block in organic synthesis for the assembly of peptides and proteins, contributing to the development of complex organic molecules and pharmaceutical compounds.
Used in Peptide Chemistry:
In peptide chemistry, FMOC-PHE(3-I)-OH is utilized as a protecting group for the amino acid phenylalanine. It shields the amine group during peptide synthesis, allowing for the controlled formation of peptide bonds. The protecting group is then removed under mild conditions to reveal the free amine, facilitating further reactions or the completion of the peptide sequence.
Used in Pharmaceutical Development:
FMOC-PHE(3-I)-OH's role in peptide synthesis makes it a valuable component in the development of pharmaceuticals. Its ability to protect and later reveal the amine group of phenylalanine is crucial for the synthesis of specific drug molecules that require precise peptide sequences.
Used in Research Laboratories:
FMOC-PHE(3-I)-OH is also used in research settings to study the properties and behavior of peptides and proteins. Its application in the synthesis of biologically active peptides aids in understanding their structure, function, and potential therapeutic applications.
Used in the Production of Radiopharmaceuticals:
In the field of nuclear medicine, FMOC-PHE(3-I)-OH, due to its iodine-containing structure, can be used in the production of radiopharmaceuticals. The iodine atom can be replaced with a radioactive isotope, enabling the development of tracers for diagnostic imaging and therapy.
Used in Chemical Education:
FMOC-PHE(3-I)-OH serves as an educational tool in teaching the principles of organic synthesis, peptide chemistry, and the use of protecting groups in the synthesis of complex molecules, providing hands-on experience for students in chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 210282-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,2,8 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 210282-31:
(8*2)+(7*1)+(6*0)+(5*2)+(4*8)+(3*2)+(2*3)+(1*1)=78
78 % 10 = 8
So 210282-31-8 is a valid CAS Registry Number.

210282-31-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(3-iodophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-iodophenyl)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:210282-31-8 SDS

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