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155892-27-6

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155892-27-6 Usage

General Description

FMOC-O-BUTYL-L-TYROSINE N-HYDROXYSUCCINIMIDE ESTER is a chemical compound commonly used in peptide synthesis and other biochemical research applications. It is a derivative of the amino acid tyrosine, featuring a butyl ester group and a hydroxysuccinimide moiety. The FMOC (9-fluorenylmethyloxycarbonyl) protecting group at the N-terminus of the tyrosine residue makes it easily removable under mild acidic conditions, allowing for the synthesis of complex peptides. The N-hydroxysuccinimide ester serves as an efficient coupling reagent, facilitating the formation of peptide bonds between the tyrosine derivative and other amino acids. The chemical is highly reactive and should be handled with caution in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 155892-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 155892-27:
(8*1)+(7*5)+(6*5)+(5*8)+(4*9)+(3*2)+(2*2)+(1*7)=166
166 % 10 = 6
So 155892-27-6 is a valid CAS Registry Number.

155892-27-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dioxopyrrolidin-1-yl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoate

1.2 Other means of identification

Product number -
Other names Fmoc-L-Tyr(tBu)-OSu

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:155892-27-6 SDS

155892-27-6Relevant articles and documents

Site-Specific Incorporation of Multiple Thioamide Substitutions into a Peptide Backbone via Solid Phase Peptide Synthesis

Yang, Jinhua,Wang, Changliu,Yao, Chaochao,Chen, Chunqiu,Hu, Yafang,He, Guifeng,Zhao, Junfeng

, p. 1484 - 1494 (2020/01/02)

Among various peptide modification strategies, thioamide substitution by replacing the carbonyl oxygen atom of an amide bond with a sulfur atom constitutes an invaluable tool for chemical biology, for use in peptide drug discovery and protein structure-fu

Somatostatin receptor-binding peptides labeled with technetium-99m: Chemistry and initial biological studies

Pearson, Daniel A.,Lister-James, John,McBride, William J.,Wilson, David M.,Martel, Lawrence J.,Civitello, Edgar R.,Taylor, John E.,Moyer, Brian R.,Dean, Richard T.

, p. 1361 - 1371 (2007/10/03)

The synthesis of peptides which possess a high affinity for the somatostatin receptor and contain a chelator for the radionuclide technetium- 99m is described. The target compounds were designed such that they would form stable, oxotechnetium(V) chelate c

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