Boc-Phe(2-Br)-OH - ≥98% , CAS No.261165-02-0

CAS: 261165-02-0 Cat. No.: B101633 Fórmula: C14H18BrNO4 Peso molecular: 344.2 Número EC: 863-147-7
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
(S)-3-(2-bromophenyl)-2-(tert-butoxycarbonyl)propanoic acid | (S)-3-(2-BROMOPHENYL)-2-(TERT-BUTOXYCARBONYLAMINO)PROPANOIC ACID | (S)-3-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid | (2S)-3-(2-bromophenyl)-2-{[(tert-butoxy)carbonyl]amino}pr
Storage
Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
500mg
B101633-500mg
—
2 Disponible
8,59€
1g
B101633-1g
—
5 Disponible
9,46€
5g
B101633-5g
—
4 Disponible

18,14€

27,68€
Guardar 9,55 € (34.48%)
25g
B101633-25g
—
2 Disponible

78,01€

117,06€
Guardar 39,05 € (33.36%)
100g
B101633-100g
—
1 Disponible

231,60€

347,88€
Guardar 116,28 € (33.42%)
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.

Specifications

Sinónimos
(S)-3-(2-bromophenyl)-2-(tert-butoxycarbonyl)propanoic acid | (S)-3-(2-BROMOPHENYL)-2-(TERT-BUTOXYCARBONYLAMINO)PROPANOIC ACID | (S)-3-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid | (2S)-3-(2-bromophenyl)-2-{[(tert-butoxy)carbonyl]amino}pr
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488192589
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192589
Sonrisas canónicasCC(C)(C)OC(=O)NC(CC1=CC=CC=C1Br)C(=O)O
IUPAC Name(2S)-3-(2-bromophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
InChIKeyXDJSTMCSOXSTGZ-NSHDSACASA-N
INCHI1S/C14H18BrNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1Br)C(=O)O
WGK Alemania 3
Peso molecular 344.2
Reaxy-Rn 29883771
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=29883771&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 Phenylpropanoic acids  Amphetamines and derivatives  Bromobenzenes  Aryl bromides  Carbamate esters  Organic carbonic acids and derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalanine or derivatives - 3-phenylpropanoic-acid - Amphetamine or derivatives - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Carbonic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - 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.

10 results found

Lot NumberCertificate TypeFechaArticulo
A1304006Certificate of AnalysisJan 07, 2026 B101633
I2519100Certificate of AnalysisOct 11, 2025 B101633
G2305415Certificate of AnalysisApr 08, 2025 B101633
G2305416Certificate of AnalysisApr 08, 2025 B101633
G2305417Certificate of AnalysisApr 08, 2025 B101633
G2305418Certificate of AnalysisApr 08, 2025 B101633
G2305419Certificate of AnalysisApr 08, 2025 B101633
G2305420Certificate of AnalysisApr 08, 2025 B101633
G2305437Certificate of AnalysisApr 08, 2025 B101633
G2305442Certificate of AnalysisApr 08, 2025 B101633
Propiedades químicas y físicas
Peso molecular344.200 g/mol
XLogP33.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count6
Exact Mass343.042 Da
Monoisotopic Mass343.042 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count20
Formal Charge0
Complexity354.000
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
Preguntas frecuentes y artículos
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.