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Fmoc-(S)-3-Amino-3-phenylpropionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209252-15-3

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209252-15-3 Usage

Chemical Properties

white to light yellow powder

Check Digit Verification of cas no

The CAS Registry Mumber 209252-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,5 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209252-15:
(8*2)+(7*0)+(6*9)+(5*2)+(4*5)+(3*2)+(2*1)+(1*5)=113
113 % 10 = 3
So 209252-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H21NO4/c26-23(27)14-22(16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/p-1/t22-/m1/s1

209252-15-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (00396)  Fmoc-β-D-Phe-OH  ≥98.0% (HPLC)

  • 209252-15-3

  • 00396-100MG

  • 1,001.52CNY

  • Detail

209252-15-3SDS

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 Fmoc-(S)-3-Amino-3-phenylpropionic acid

1.2 Other means of identification

Product number -
Other names (S)-N-Fmoc-3-Amino-3-phenylpropanoic acid

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:209252-15-3 SDS

209252-15-3Relevant academic research and scientific papers

Solid phase synthesis of novel α/β-tetrapeptides, electrospray ionization mass spectrometric evaluation of their metal cation complexation behavior, and conformational analysis using density functional theory (DFT)

Bandala, Yamir,Avina, Judit,Gonzalez, Tania,Rivero, Ignacio A.,Juaristi, Eusebio

, p. 349 - 358 (2008/12/20)

Thirty-four novel α/β-tetrapeptides (1-34) have been prepared employing solid-phase and in-parallel synthetic protocols. α/β- Tetrapeptides 1-34 were prepared by a combination of three α-amino acid residues (alanine (Ala), phenylalanine (Phe), and isoleucine (Ile)) with one β-amino acid residue (β3-homophenylglycine). The corresponding complexes of several selected α/β-tetrapeptides with alkali, alkaline earth, and transition metals, [tP + M+], were evaluated using ion electrospray-ionization mass spectrometry (ESI-MS). According to the results from analysis of mixtures, we can conclude that the position of the β-amino acid is determinant in the affinity toward different metal cations. Computational modeling (DFT, B3LYP 6-311++G) provided useful information regarding the most likely coordination sites of the metal ions on the receptor α/β-tetrapeptide 12, HO2C-α- Phe-α-Phe-α-Ile-β3-hPhg-NH2, as well as the conformational changes induced by the metal upon [tP + M+] complex formation. Copyright

A convenient method for the synthesis of β-amino acids via the Arndt-Eistert approach using p-toluenesulphonyl chloride as a carboxylic group activating agent

Vasanthakumar, Ganga-Ramu,Suresh Babu, Vommina V.

, p. 651 - 657 (2007/10/03)

A simple method for the synthesis of Z-/Boc-/Fmoc-protected β-amino acids by the Arndt-Eistert approach employing p-toluenesulphonyl chloride for the activation of the carboxyl group of Nα-protected amino acid is described. The method is rapid and gave good yields with opitical purity.

Synthesis of Fmoc-β-homoamino acids by ultrasound-promoted wolff rearrangement

Müller, Annett,Vogt, Carla,Sewald, Norbert

, p. 837 - 841 (2007/10/03)

A highly efficient protocol for Amdt-Eistert chain elongation of the base-labile fluorenylmethoxycarbonyl (Fmoc) protected α-amino acids by Ag+- catalyzed, ultrasound-promoted Wolff rearrangement of the corresponding α- diazo ketones at room temperature is described. The enantiomeric purity of the products was examined by capillary zone electrophoresis with chiral buffer systems.

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