8.53042
Boc-Tyr(2,6-di-Cl-Bzl)-OH
Novabiochem®
别名:
Boc-Tyr(2,6-di-Cl-Bzl)-OH, N-α-t.-Boc-O-2,6-dichlorobenzyl-L-tyrosine
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关于此项目
经验公式（希尔记法）:
C21H23Cl2NO5
化学文摘社编号:
分子量:
440.32
UNSPSC Code:
12352209
EC Index Number:
254-876-6
NACRES:
NA.22
MDL number:
产品名称
Boc-Tyr(2,6-di-Cl-Bzl)-OH, Novabiochem®
SMILES string
Clc1c(c(ccc1)Cl)COc2ccc(cc2)CC(NC(=O)OC(C)(C)C)C(=O)O
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
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
Quality Level
Analysis Note
Colour (visual): white to slight yellow to beige
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
To see the solvent systems used for TLC of Novabiochem® products please click here.
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
To see the solvent systems used for TLC of Novabiochem® products please click here.
General description
Building block for introduction of tyrosine amino-acid residues by Boc SPPS.
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Boc SPPS
Other Notes
Replaces: 04-12-0014
Legal Information
Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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实验方案
Anhydrous HF is the preferred reagent for peptide cleavage from Boc-based resins, versatile and effective for various peptide synthesis.
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