945669-52-3

Basic information

• Product Name: (S)-3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID
• Synonyms: (S)-3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID;3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID;L-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-2,6-dimethyl-O-(phenylmethyl)-;(S)-3-(4-(Benzyloxy)-2,6-dimethylphenyl)-2-(tert-butoxycarbonylamino)propanoic acid;(S)-O-BENZYL-N-BOC-2,6-DIMETHYL TYROSINE
• CAS NO: 945669-52-3
• Molecular Formula: C₂₃H₂₉NO₅
• Molecular Weight: 399.48
• Mol File: 945669-52-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 582.4°C at 760 mmHg
• Flash Point: 306°C
• Appearance: /
• Density: 1.154g/cm³
• Vapor Pressure: 2.09E-14mmHg at 25°C
• Refractive Index: 1.556
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (S)-3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID(945669-52-3)
• EPA Substance Registry System: (S)-3-(4-BENZYLOXY-2,6-DIMETHYL-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID(945669-52-3)

Safety Data

• Hazardous Substances Data: 945669-52-3(Hazardous Substances Data)

Usage

General Description

(S)-3-(4-benzyloxy-2,6-dimethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid, also known as Boc-3-iodotyrosine, is a chemical compound commonly used in solid-phase peptide synthesis. It is a derivative of tyrosine and contains a benzyloxy group as well as a tert-butoxycarbonyl (Boc) protecting group. Boc-3-iodotyrosine is a versatile building block in the synthesis of complex peptides and proteins, playing a key role in the development of new pharmaceuticals, diagnostics, and biotechnology products. It is an important tool for peptide and protein chemistry, enabling the creation of precise and specific peptide sequences for a wide range of biological and medical applications.

InChI:InChI=1/C23H29NO5/c1-15-11-18(28-14-17-9-7-6-8-10-17)12-16(2)19(15)13-20(21(25)26)24-22(27)29-23(3,4)5/h6-12,20H,13-14H2,1-5H3,(H,24,27)(H,25,26)/t20-/m0/s1

Upstream product

• 95741-44-9 1-((4-bromo-3,5-dimethylphenoxy)methyl)benzene 

Downstream Products

• 123715-02-6 H-Dmt 

Relevant articles and documents

Method for Preparing Unnatural Amino Acids

The present invention relates to a manufacturing method of unnatural amino acids and unnatural amino acids manufactured thereby. Specifically, the present invention relates to an asymmetric synthesis method which can manufacture unnatural amino acids having significantly high optical purity, and to the unnatural amino acids manufactured thereby. A manufacturing method of unnatural amino acids represented by chemical formula 6 or chemical formula 7 comprises the steps of: synthesizing a compound represented by chemical formula 4 or chemical formula 5; manufacturing a diol compound; and manufacturing a carboxylic acid compound.COPYRIGHT KIPO 2016