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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Boc-Trp-OH - ≥98% , CAS No.13139-14-5
Disponível para encomenda
Synonyms
AS-12736 | Boc-trytophan | CHEBI:183830 | tert-Butoxycarbonyltryptophan | L-Tryptophan, N-((1,1-dimethylethoxy)carbonyl)- | Nalpha-t-butoxycarbonyl-L-tryptophan | N-(tert-Butoxycarbonyl)-L-tryptophan | 2-(2-Fluorophenoxy)acetic | BOC-L-TRYPTOPHANE | EINEC
Storage
Room temperature,Argon charged
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Argon charged Ships Normal 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
AS-12736 | Boc-trytophan | CHEBI:183830 | tert-Butoxycarbonyltryptophan | L-Tryptophan, N-((1,1-dimethylethoxy)carbonyl)- | Nalpha-t-butoxycarbonyl-L-tryptophan | N-(tert-Butoxycarbonyl)-L-tryptophan | 2-(2-Fluorophenoxy)acetic | BOC-L-TRYPTOPHANE | EINEC
Especificações e pureza
≥98%
Condições de armazenamento de armazenamento
Room temperature,Argon charged
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488186159
Sorrisos canónicos
CC(C)(C)OC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O
IUPAC Name
(2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
InChIKey
NFVNYBJCJGKVQK-ZDUSSCGKSA-N
INCHI
1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/t13-/m0/s1
SMILES isoméricas
CC(C)(C)OC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=493747&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 Organoheterocyclic compounds Classe Indoles and derivatives Subclass Indolyl carboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Indolyl carboxylic acids and derivatives Alternative Parents Alpha amino acids and derivatives 3-alkylindoles Substituted pyrroles Benzenoids Heteroaromatic compounds Carbamate esters Organic carbonic acids and derivatives Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Indolyl carboxylic acid derivative - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Substituted pyrrole - Benzenoid - Pyrrole - Carbamic acid ester - Heteroaromatic compound - Carbonic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Organic oxide - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Air sensitive; Light sensitive Rotação específica [α] -17.5 ° (C=2, DMF) Ponto de inflamação (°F) 132.8 °F Ponto de inflamação (°C) 56 °C Ponto de fusão (°C) 134-138°C Peso molecular 304.340 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 6 Exact Mass 304.142 Da Monoisotopic Mass 304.142 Da Topological Polar Surface Area 91.400 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 419.000 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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