Basic information

Product Name: FMOC-PHE(3-I)-OH
Synonyms: FMOC-PHE(3-I)-OH;FMOC-PHE(2-I)-OH;FMOC-S-PHE(3-I)-OH;FMOC-2-IODO-L-PHENYLALANINE;FMOC-3-IODO-L-PHENYLALANINE;FMOC-L-3-IODOPHENYLALANINE;FMOC-L-PHE(3-I);FMOC-L-PHE(3-I)-OH
CAS NO:210282-32-9
Molecular Formula: C24H20INO4
Molecular Weight: 513.32
EINECS: N/A
Product Categories: Amino Acid Derivatives;Amino Acids
Mol File: 210282-32-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: Store at 0-5°C
Solubility: N/A
CAS DataBase Reference: FMOC-PHE(3-I)-OH(CAS DataBase Reference)
NIST Chemistry Reference: FMOC-PHE(3-I)-OH(210282-32-9)
EPA Substance Registry System: FMOC-PHE(3-I)-OH(210282-32-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 210282-32-9(Hazardous Substances Data)

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Usage
SDS
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210282-32-9 Usage

Uses

Used in Pharmaceutical Industry:
FMOC-PHE(3-I)-OH is used as a building block in the synthesis of peptides for various therapeutic applications. Its protective FMOC group ensures that the amino acid's reactive sites remain stable during the assembly process, which is crucial for the development of effective peptide-based drugs.
Used in Biotechnological Applications:
FMOC-PHE(3-I)-OH is used as a component in the construction of complex biological molecules, such as proteins and enzymes. The iodine atom in FMOC-PHE(3-I)-OH can be utilized for further modifications, enabling the creation of novel biotechnological products with enhanced properties.
Used in Peptide Synthesis:
FMOC-PHE(3-I)-OH is used as a protected amino acid in the process of peptide synthesis. Its incorporation into peptide structures during the assembly of amino acid chains is facilitated by the protective FMOC group, which prevents unwanted side reactions and ensures the correct formation of the desired peptide sequence.
Used in Research and Development:
FMOC-PHE(3-I)-OH is used as a research tool in the study of peptide chemistry and related fields. Its stability and resistance to racemization make it an important compound for investigating the properties and behavior of peptides, as well as for developing new methods and techniques in peptide synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 210282-32-9 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 210282-32:
(8*2)+(7*1)+(6*0)+(5*2)+(4*8)+(3*2)+(2*3)+(1*2)=79
79 % 10 = 9
So 210282-32-9 is a valid CAS Registry Number.

210282-32-9SDS

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-(2-iodophenyl)propanoic acid

1.2 Other means of identification

Product number	-
Other names	Fmoc-2-iodo-l-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:210282-32-9 SDS

210282-32-9Upstream product

210282-32-9Downstream Products

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