8.53042
Boc-Tyr(2,6-di-Cl-Bzl)-OH
Novabiochem®
Synonym(s):
Boc-Tyr(2,6-di-Cl-Bzl)-OH, N-α-t.-Boc-O-2,6-dichlorobenzyl-L-tyrosine
About This Item
Recommended Products
Quality Level
product line
Novabiochem®
Assay
≥98% (TLC)
form
powder
reaction suitability
reaction type: Boc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
functional group
hydroxyl
storage temp.
2-30°C
InChI
1S/C21H23Cl2NO5/c1-21(2,3)29-20(27)24-18(19(25)26)11-13-7-9-14(10-8-13)28-12-15-16(22)5-4-6-17(15)23/h4-10,18H,11-12H2,1-3H3,(H,24,27)(H,25,26)
InChI key
DODHIGHXRDNRPP-UHFFFAOYSA-N
General description
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS
Linkage
Analysis Note
Appearance of substance (visual): powder
Identity (IR): conforms
Optical rotation α 25/D (c=2 in ethanol): +17.5 - +22.5 °
Purity (TLC(011A)): ≥ 98 %
Purity (TLC(0811)): ≥ 98 %
Solubility (1 mmole in 2 ml DMF): clearly soluble
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Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Protocols
The most popular reagent for cleavage of peptides from Boc-based resins is anhydrous HF. Of all the cleavage procedures HF appears to be the most versatile and least harmful to a wide variety of peptides synthesized on Boc-based resins.
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