Boc-Ser-OMe - ≥95% , CAS No.2766-43-0

CAS: 2766-43-0 Cat. No.: B116726 Peso molecular: 219.23 Beilstein Registry Number: 3545389 Número EC: 690-499-7
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
HY-32688 | .beta.-Cyanoethyl acrylate | DTXSID30427089 | methyl (tert-butoxycarbonyl)-L-serinate | Boc-L-Ser-OMe | SCHEMBL313780 | (5)-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate | methyl N-(tert-butoxycarbonyl)-L-serinate | N-(tert-butoxyca
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
B116726-1g
3

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
B116726-5g
2

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
25g
B116726-25g
2

36,90US$

55,90US$
Guardar 19,00 US$ (33.99%)
100g
B116726-100g
2

61,90US$

92,90US$
Guardar 31,00 US$ (33.37%)
500g
B116726-500g
1

157,90US$

236,90US$
Guardar 79,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
HY-32688 | .beta.-Cyanoethyl acrylate | DTXSID30427089 | methyl (tert-butoxycarbonyl)-L-serinate | Boc-L-Ser-OMe | SCHEMBL313780 | (5)-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate | methyl N-(tert-butoxycarbonyl)-L-serinate | N-(tert-butoxyca
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%
Nombres e identificadores
Pubchem Sid504764606
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764606
Sonrisas canónicasCC(C)(C)OC(=O)NC(CO)C(=O)OC
IUPAC Namemethyl (2S)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
InChIKeySANNKFASHWONFD-LURJTMIESA-N
INCHI1S/C9H17NO5/c1-9(2,3)15-8(13)10-6(5-11)7(12)14-4/h6,11H,5H2,1-4H3,(H,10,13)/t6-/m0/s1
Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CO)C(=O)OC
WGK Alemania 3
Peso molecular 219.23
Beilstein 3545389
Reaxy-Rn 1964834
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1964834&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 ParentAlpha amino acid esters
Alternative Parents Serine and derivatives  Beta hydroxy acids and derivatives  Methyl esters  Carbamate esters  Monocarboxylic acids and derivatives  Primary alcohols  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha-amino acid ester - Serine or derivatives - Beta-hydroxy acid - Hydroxy acid - Methyl ester - Carbamic acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Alcohol - Organooxygen compound - Organonitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
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
E2218013Certificate of AnalysisMar 10, 2026 B116726
E2218019Certificate of AnalysisMar 10, 2026 B116726
E2218020Certificate of AnalysisMar 10, 2026 B116726
E2218022Certificate of AnalysisMar 10, 2026 B116726
E2218023Certificate of AnalysisMar 10, 2026 B116726
A1314060Certificate of AnalysisAug 05, 2024 B116726
C2522053Certificate of AnalysisMar 07, 2022 B116726
Propiedades químicas y físicas
SensibilidadAir Sensitive
Índice de refracción1.452
Rotación específica [α]-18 ° (C=5, MeOH)
Punto de inflamación (°F)235.4 °F
Punto de inflamación (°C)113 °C
Peso molecular219.230 g/mol
XLogP30.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass219.111 Da
Monoisotopic Mass219.111 Da
Topological Polar Surface Area84.900 Ų
Heavy Atom Count15
Formal Charge0
Complexity233.000
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
Citations of This Product
Referencias
1. Bu Xiaohai, Zhou Yuming, Zhang Tao, He Man.  (2014)  Preparation of optically active substituted polyacetylene@CdSe quantum dots composites and their application for low infrared emissivity.  JOURNAL OF MATERIALS SCIENCE,  49  (20): (7133-7142).  [PMID:] [10.1007/s10853-014-8421-y]
2. Xiaohai Bu, Yuming Zhou, Zhenjie Chen, Man He, Tao Zhang.  (2014)  Optically active amino acid-based polyacetylenes: Effect of tunable helical conformation on infrared emissivity property.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2014.05.006]
3. Xiaohai Bu, Yuming Zhou, Tao Zhang, Yongjuan Wang, Zewu Zhang, Man He.  (2014)  Optically active substituted polyacetylene@carbon nanotube hybrids: Preparation, characterization and infrared emissivity property study.  JOURNAL OF SOLID STATE CHEMISTRY,      [PMID:] [10.1016/j.jssc.2014.04.011]
4. Xiaohai Bu, Yuming Zhou, Man He, Zhenjie Chen, Tao Zhang.  (2013)  Optically active SiO2/TiO2/polyacetylene multilayered nanospheres: Preparation, characterization, and application for low infrared emissivity.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2013.10.053]
Calculadoras de soluciones
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