Boc-Phe-OMe - ≥98% , CAS No.51987-73-6

CAS: 51987-73-6 Cat. No.: B136644 Fórmula: C6H5CH2CH[NHCO2C(CH3)3]CO2CH3 Peso molecular: 279.33 Beilstein Registry Number: 3061910 Número EC: 628-049-9
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
(R-(R*,S*))-6-Bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-1-octene | N-tert-butoxycarbonyl-L-phenylalanine methyl ester | AC-24155 | SDSWSVBXRBXPRL-LBPRGKRZSA-N | AM82170 | (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate | N-[(1,1-dimethyl
Storage
Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
1g
B136644-1g
—
5 Disponible
8,59€
5g
B136644-5g
—
4 Disponible
9,46€
25g
B136644-25g
—
2 Disponible

20,74€

31,15€
Guardar 10,41 € (33.43%)
100g
B136644-100g
Fabricado bajo pedido · 8–12 semanas

58,92€

88,42€
Guardar 29,50 € (33.37%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Boc-Phe-OMe is a a Boc-protected amino acid derivative
A Boc-protected amino acid derivative

Specifications

Sinónimos
(R-(R*,S*))-6-Bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-1-octene | N-tert-butoxycarbonyl-L-phenylalanine methyl ester | AC-24155 | SDSWSVBXRBXPRL-LBPRGKRZSA-N | AM82170 | (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate | N-[(1,1-dimethyl
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488196392
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488196392
Sonrisas canónicasCC(C)(C)OC(=O)NC(CC1=CC=CC=C1)C(=O)OC
IUPAC Namemethyl (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoate
InChIKeySDSWSVBXRBXPRL-LBPRGKRZSA-N
INCHI1S/C15H21NO4/c1-15(2,3)20-14(18)16-12(13(17)19-4)10-11-8-6-5-7-9-11/h5-9,12H,10H2,1-4H3,(H,16,18)/t12-/m0/s1
Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)OC
WGK Alemania 3
Peso molecular 279.33
Beilstein 3061910
Reaxy-Rn 2749835
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2749835&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentPhenylalanine and derivatives
Alternative Parents Alpha amino acid esters  Amphetamines and derivatives  Fatty acid esters  Methyl esters  Carbamate esters  Monocarboxylic acids and derivatives  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalanine or derivatives - Alpha-amino acid ester - Amphetamine or derivatives - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Methyl ester - Carbamic acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeFechaArticulo
C23151100Certificate of AnalysisSep 01, 2026 B136644
E1526039Certificate of AnalysisJul 07, 2026 B136644
F2611136Certificate of AnalysisJun 16, 2026 B136644
E2327471Certificate of AnalysisMar 05, 2025 B136644
C2201119Certificate of AnalysisDec 25, 2023 B136644
C2201121Certificate of AnalysisDec 25, 2023 B136644
D2001005Certificate of AnalysisFeb 19, 2022 B136644
Propiedades químicas y físicas
Rotación específica [α]-3° (C=2,MeOH)
Punto de inflamación (°F)235.4 °F
Punto de inflamación (°C)113 °C
Punto de fusión (°C)36-40°C
Peso molecular279.330 g/mol
XLogP32.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass279.147 Da
Monoisotopic Mass279.147 Da
Topological Polar Surface Area64.599 Ų
Heavy Atom Count20
Formal Charge0
Complexity329.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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