Basic Description

Synonyms	(s)-2-(fmoc-amino)-5-phenyl-4-pentenoic acid \| Fmoc-3-styryl-D-alanine \| SCHEMBL2308300 \| SCHEMBL2308312 \| (R)-N-Fmoc-Styrylalanine \| E70567 \| AC-9974 \| J-014127 \| 1211448-58-6 \| (2R)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-5-phenyl-4-pentenoic acid \|
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Fmoc-∫-styryl-D-Ala-OH is an Fmoc protected alanine derivative that is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Alanine is one of the simplest amino acids - a methyl group as the side chain. This small side chain confers a high degree of flexibility (second only to glycine) when incorporated into a polypeptide chain. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Fluorenes

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Fluorenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Fluorenes
Alternative Parents	Alpha amino acids and derivatives Styrenes Medium-chain fatty acids Amino fatty acids Unsaturated fatty acids Carbamate esters Monocarboxylic acids and derivatives Carboxylic acids Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Fluorene - Alpha-amino acid or derivatives - Medium-chain fatty acid - Styrene - Amino fatty acid - Monocyclic benzene moiety - Fatty acyl - Fatty acid - Unsaturated fatty acid - Carbamic acid ester - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504763920
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504763920
IUPAC Name	(E,2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-phenylpent-4-enoic acid
INCHI	InChI=1S/C26H23NO4/c28-25(29)24(16-8-11-18-9-2-1-3-10-18)27-26(30)31-17-23-21-14-6-4-12-19(21)20-13-5-7-15-22(20)23/h1-15,23-24H,16-17H2,(H,27,30)(H,28,29)/b11-8+/t24-/m1/s1
InChIKey	ZFMHHKMOLFNMMV-NOENIZQJSA-N
Smiles	C1=CC=C(C=C1)C=CCC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Isomeric SMILES	C1=CC=C(C=C1)/C=C/C[C@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
PubChem CID	5702631
Molecular Weight	413.47

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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4 results found

Lot Number	Certificate Type	Date	Item
F2519090	Certificate of Analysis	Aug 19, 2022	F350471
K2225562	Certificate of Analysis	Aug 19, 2022	F350471
K2225563	Certificate of Analysis	Aug 19, 2022	F350471
K2225536	Certificate of Analysis	Aug 19, 2022	F350471

Chemical and Physical Properties

Molecular Weight	413.500 g/mol
XLogP3	5.300
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	8
Exact Mass	413.163 Da
Monoisotopic Mass	413.163 Da
Topological Polar Surface Area	75.600 Å²
Heavy Atom Count	31
Formal Charge	0
Complexity	619.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

Documents & Articles

Solid-Phase Peptide Synthesis (SPPS) — Efficient Strategies and Innovative Techniques

Categories: Technical articles

Tags:

Chemical synthesis Amino acids Protein Biology Acids Solvents Carbohydrates Peptides Peptide synthesis reagents Organic blocks SPPS Peptide synthesis Protection groups

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SKU	Size	Availability	Price
F350471-250mg	250mg	3	$148.90
F350471-1g	1g	2	$533.90
F350471-5g	5g	2	$2,400.90

Fmoc-β-styryl-D-Ala-OH - 98%, high purity , CAS No.215190-23-1