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FMOC-D-GLU-OTBU is a chemical compound that features a FMOC (fluorenylmethyloxycarbonyl) protecting group, a D (dextro) configuration of the glutamic acid, and an OTBU (tert-butyl ester) protecting group. FMOC-D-GLU-OTBU is designed for use in peptide synthesis, where the FMOC group shields the amino group of the amino acid, facilitating the stepwise assembly of peptides. The D configuration of the glutamic acid denotes a mirror image of the L configuration commonly found in biological systems, while the OTBU group serves to protect the carboxylic acid group of the glutamic acid. FMOC-D-GLU-OTBU is a versatile compound utilized in both peptide synthesis and organic chemistry research.

109745-15-5

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109745-15-5 Usage

Uses

Used in Peptide Synthesis:
FMOC-D-GLU-OTBU is used as a protected amino acid building block for the synthesis of peptides. The FMOC protecting group allows for the stepwise addition of amino acids in a controlled manner, while the OTBU group shields the carboxylic acid group, preventing unwanted side reactions during the synthesis process.
Used in Organic Chemistry Research:
FMOC-D-GLU-OTBU is used as a research compound in organic chemistry to study the properties and reactions of protected amino acids. The D configuration of the glutamic acid provides insights into the behavior of non-standard amino acid configurations in chemical reactions and their potential applications in the development of new pharmaceuticals and bioactive molecules.
Used in Pharmaceutical Development:
FMOC-D-GLU-OTBU is used as a precursor in the development of new pharmaceuticals, particularly in the synthesis of peptide-based drugs. FMOC-D-GLU-OTBU's protected groups enable the creation of complex peptide structures with specific biological activities, which can be further optimized for therapeutic applications.
Used in Biochemistry and Molecular Biology:
FMOC-D-GLU-OTBU is used as a tool in biochemical and molecular biology research to study protein structure, function, and interactions. FMOC-D-GLU-OTBU can be incorporated into peptides and proteins to investigate the effects of D-amino acids on protein folding, stability, and binding properties.

Check Digit Verification of cas no

The CAS Registry Mumber 109745-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,4 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109745-15:
(8*1)+(7*0)+(6*9)+(5*7)+(4*4)+(3*5)+(2*1)+(1*5)=135
135 % 10 = 5
So 109745-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H27NO6/c1-24(2,3)31-22(28)20(12-13-21(26)27)25-23(29)30-14-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,19-20H,12-14H2,1-3H3,(H,25,29)(H,26,27)/t20-/m1/s1

109745-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-D-Glu-OtBu

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:109745-15-5 SDS

109745-15-5Relevant articles and documents

Synthesis of cell-wall analogues of vancomycin-resistant Enterococci using solid phase peptide synthesis

Cho, Younghoon R.,Entress, Richard M. H.,Williams, Dudley H.

, p. 5229 - 5232 (1997)

A convenient method for the direct coupling of lithium D-lactate to 2-chlorotrityl chloride resin enabled the rapid and efficient solid phase synthesis of bacterial cell-wall precursor analogues (depsipeptides) found in vancomycin-resistant enterococci (VRE).

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