Boc-Tyr-OMe - ≥99% , CAS No.4326-36-7

CAS: 4326-36-7 Cat. No.: B110968 Peso molecular: 295.33 Número EC: 805-703-3
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
(S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester | methyl N-(tert-butoxycarbonyl)-L-tyrosinate | NQIFXJSLCUJHBB-LBPRGKRZSA-N | NSC 71049 | STK399782 | LF-0551 | 1,2,4-Triazolopyridin-3-one | N-Boc-L-tyrosine Methyl Ester | B
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
B110968-5g
4
9,90US$
25g
B110968-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
24,90US$
100g
B110968-100g
1
65,90US$
500g
B110968-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
264,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
(S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester | methyl N-(tert-butoxycarbonyl)-L-tyrosinate | NQIFXJSLCUJHBB-LBPRGKRZSA-N | NSC 71049 | STK399782 | LF-0551 | 1, 2, 4-Triazolopyridin-3-one | N-Boc-L-tyrosine Methyl Ester | B
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488196107
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488196107
Sonrisas canónicasCC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)O)C(=O)OC
IUPAC Namemethyl (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
InChIKeyNQIFXJSLCUJHBB-LBPRGKRZSA-N
INCHI1S/C15H21NO5/c1-15(2,3)21-14(19)16-12(13(18)20-4)9-10-5-7-11(17)8-6-10/h5-8,12,17H,9H2,1-4H3,(H,16,19)/t12-/m0/s1
Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)OC
WGK Alemania 3
Peso molecular 295.33
Reaxy-Rn 2881359
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2881359&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 ParentTyrosine and derivatives
Alternative Parents Phenylalanine and derivatives  Alpha amino acid esters  Amphetamines and derivatives  Fatty acid esters  1-hydroxy-2-unsubstituted benzenoids  Methyl esters  Carbamate esters  Monocarboxylic acids and derivatives  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Tyrosine or derivatives - Phenylalanine or derivatives - Alpha-amino acid ester - Amphetamine or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Phenol - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Methyl ester - Carbamic acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as tyrosine and derivatives. These are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine 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.

8 results found

Lot NumberCertificate TypeFechaArticulo
J1411105Certificate of AnalysisApr 15, 2026 B110968
J2123146Certificate of AnalysisAug 11, 2025 B110968
J2123150Certificate of AnalysisAug 11, 2025 B110968
K2505205Certificate of AnalysisJul 13, 2024 B110968
K2505206Certificate of AnalysisJul 13, 2024 B110968
F1924238Certificate of AnalysisApr 12, 2023 B110968
B2428018Certificate of AnalysisOct 27, 2021 B110968
E2325149Certificate of AnalysisOct 27, 2021 B110968
Propiedades químicas y físicas
SolubilidadSolubility in Methanol almost transparency
Rotación específica [α]50 ° (C=1, MeOH)
Punto de fusión (°C)100-104°C
Peso molecular295.330 g/mol
XLogP31.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count7
Exact Mass295.142 Da
Monoisotopic Mass295.142 Da
Topological Polar Surface Area84.900 Ų
Heavy Atom Count21
Formal Charge0
Complexity356.000
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
Citations of This Product
Referencias
1. Shan Yuyao, Qi Wei, Wang Mengfan, Su Rongxin, He Zhimin.  (2018)  Kinetically Controlled Carboxypeptidase-Catalyzed Synthesis of Novel Antioxidant Dipeptide Precursor BOC-Tyr-Ala.  TRANSACTIONS OF TIANJIN UNIVERSITY,  24  (6): (513-521).  [PMID:] [10.1007/s12209-018-0166-2]
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