103213-31-6

Basic information

• Product Name: FMOC-3,5-DIIODO-L-TYROSINE
• Synonyms: FMOC-3,5-DIIODO-L-TYROSINE;FMOC-3,5-DIIODO-TYR-OH;FMOC-3,5-DIIODO-TYROSINE;FMOC-L-TYR(3,5-I2)-OH;FMOC-TYR(3,5-DI-I)-OH;FMOC-TYR(3,5-I2)-OH;N-9-Fluorenylmethoxycarbonyl-3,5-diiodo-L-tyrosine;Fmoc-Tyr(3',5'-I2)
• CAS NO: 103213-31-6
• Molecular Formula: C24H19I2NO5
• Molecular Weight: 655.22
• Product Categories: Amino Acids
• Mol File: 103213-31-6.mol

Chemical Properties

• Boiling Point: 687.3oC at 760 mmHg
• Flash Point: 369.5oC
• Appearance: White/Powder
• Density: 1.893g/cm3
• Vapor Pressure: 7.8E-20mmHg at 25°C
• Refractive Index: 1.716
• Storage Temp.: 2-8°C
• PKA: 2.78±0.10(Predicted)
• Sensitive: Light Sensitive
• BRN: 9022736
• CAS DataBase Reference: FMOC-3,5-DIIODO-L-TYROSINE(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-3,5-DIIODO-L-TYROSINE(103213-31-6)
• EPA Substance Registry System: FMOC-3,5-DIIODO-L-TYROSINE(103213-31-6)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 8
• HazardClass: IRRITANT
• Hazardous Substances Data: 103213-31-6(Hazardous Substances Data)

Usage

Uses

Used in Biochemistry and Organic Synthesis:
FMOC-3,5-DIIODO-L-TYROSINE is used as a reagent in peptide synthesis for its ability to facilitate the formation of peptide bonds and its role as a halogenated building block in organic synthesis. Its distinct chemical properties make it a versatile compound in the laboratory setting.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, FMOC-3,5-DIIODO-L-TYROSINE is utilized as a key component in the development of new drugs and therapeutic agents. Its unique structure and reactivity contribute to the design and synthesis of novel pharmaceutical compounds with potential applications in various medical fields.
Used in Medicinal Chemistry:
FMOC-3,5-DIIODO-L-TYROSINE serves as a valuable tool in medicinal chemistry for the synthesis of bioactive molecules and the modification of existing drugs to improve their efficacy, selectivity, and pharmacokinetic properties. Its presence in the synthesis process can lead to the development of more effective treatments for various diseases and conditions.

InChI:InChI=1/C24H19I2NO5/c25-19-9-13(10-20(26)22(19)28)11-21(23(29)30)27-24(31)32-12-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18/h1-10,18,21,28H,11-12H2,(H,27,31)(H,29,30)/t21-/m0/s1

Downstream Products

• 1423015-83-1 tri--tert--butyl 2,2',2''-(10--(2--((((9H--fluoren--9--yl)methoxy)carbonyl)amino)--3-(((S)--1--(tert-butoxy)--3--(4--hydroxy--3,5--diiodophenyl)-1--oxopropan--2--yl)amino)--3--oxopropyl)--1,4,7,10--tetraazacyclododecane--1,4,7--triyl)triacetate 
• 1423015-84-2 C₄₂H₇₀I₂N₆O₁₀ 
• 1423015-77-3 tri--tert-butyl 2,2',2''-(10--(2--(2--((((9H--fluoren-9-yl)methoxy)carbonyl)amino)-3--(4-hydroxy--3,5--diiodophenyl)propanamido)--3-(((S)-1-methoxy-1-oxopropan-2-yl)amino)-3-oxopropyl)-1,4,7,10-tetraazacyclododecane-1,4,7--triyl)triacetate