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· · COA & SDS available for every product · Same-day shipping on in-stock items Fmoc-4-Chloro-D-Phe-OH - ≥98% , CAS No.142994-19-2
Synonyms
(R)-3-(4-Chloro-phenyl)-2-(Fmoc-amino)-propionic acid;Fmoc-4-chloro-D-Phe-OH | Fmoc-D-Phe(4-Cl)-OH, >=98.0% (HPLC) | AC-29554 | Fmoc-(D)Phe(4-Cl)-OH | MLS001074428 | Fmoc-L-phe(4-Cl)-OH | 4-Chloro-N-Fmoc-D-phenylalanine | A807998 | Fmoc-D-Phe(4-Cl)-OH | (
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
(R)-3-(4-Chloro-phenyl)-2-(Fmoc-amino)-propionic acid;Fmoc-4-chloro-D-Phe-OH | Fmoc-D-Phe(4-Cl)-OH, >=98.0% (HPLC) | AC-29554 | Fmoc-(D)Phe(4-Cl)-OH | MLS001074428 | Fmoc-L-phe(4-Cl)-OH | 4-Chloro-N-Fmoc-D-phenylalanine | A807998 | Fmoc-D-Phe(4-Cl)-OH | (
Specifications & Purity
≥98%
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504768211 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504768211 Canonical Smiles C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC=C(C=C4)Cl)C(=O)O IUPAC Name (2R)-3-(4-chlorophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid InChIKey CQPNKLNINBUUOM-JOCHJYFZSA-N INCHI 1S/C24H20ClNO4/c25-16-11-9-15(10-12-16)13-22(23(27)28)26-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m1/s1 Isomeric SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@H](CC4=CC=C(C=C4)Cl)C(=O)O WGK Germany 3 Molecular Weight 421.87 Beilstein 8726004 Reaxy-Rn 9437839 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9437839&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Phenylalanine and derivatives Alternative Parents Fluorenes Phenylpropanoic acids Amphetamines and derivatives Chlorobenzenes Aryl chlorides Carbamate esters Monocarboxylic acids and derivatives Carboxylic acids Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic anions Molecular Framework Aromatic homopolycyclic compounds Substituents Phenylalanine or derivatives - Fluorene - 3-phenylpropanoic-acid - Amphetamine or derivatives - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Carboxylic acid - Monocarboxylic acid or derivatives - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Organic anion - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. External Descriptors Not available Data sources 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 194°C Molecular Weight 421.900 g/mol XLogP3 5.300 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 7 Exact Mass 421.108 Da Monoisotopic Mass 421.108 Da Topological Polar Surface Area 75.600 Ų Heavy Atom Count 30 Formal Charge 0 Complexity 584.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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