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224,000+ produtos de pesquisa · Triple ISO certified · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque 2-Ethoxy-1-naphthaleneboronic acid - ≥96% , CAS No.148345-64-6
Disponível para encomenda
Synonyms
2-Ethoxy-1-naphthaleneboronic acid|148345-64-6|(2-ethoxynaphthalen-1-yl)boronic acid|Boronic acid, B-(2-ethoxy-1-naphthalenyl)-|MFCD05664211|2-Ethoxynaphthalen-1-ylboronic acid|2-ETHOXY-1-NAPHTHALENEBORONICACID|SCHEMBL1642006|DTXSID50584123|QUDVXFWSKXUSMY
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Why this grade ≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Visão geral Pd-catalyzed Suzuki-Miyaura reaction
Specifications Sinónimos
2-Ethoxy-1-naphthaleneboronic acid | 148345-64-6 | (2-ethoxynaphthalen-1-yl)boronic acid | Boronic acid, B-(2-ethoxy-1-naphthalenyl)- | MFCD05664211 | 2-Ethoxynaphthalen-1-ylboronic acid | 2-ETHOXY-1-NAPHTHALENEBORONICACID | SCHEMBL1642006 | DTXSID50584123 | QUDVXFWSKXUSMY
Especificações e pureza
≥96%
Condições de armazenamento de armazenamento
Room temperature
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504768241
Sorrisos canónicos
B(C1=C(C=CC2=CC=CC=C12)OCC)(O)O
IUPAC Name
(2-ethoxynaphthalen-1-yl)boronic acid
InChIKey
QUDVXFWSKXUSMY-UHFFFAOYSA-N
INCHI
1S/C12H13BO3/c1-2-16-11-8-7-9-5-3-4-6-10(9)12(11)13(14)15/h3-8,14-15H,2H2,1H3
SMILES isoméricas
B(C1=C(C=CC2=CC=CC=C12)OCC)(O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=19026841&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 Benzenoids Classe Naphthalenes Subclass Not available Intermediate Tree Nodes Not available Direct Parent Naphthalenes Alternative Parents Alkyl aryl ethers Boronic acids Organic metalloid salts Organoboron compounds Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Naphthalene - Alkyl aryl ether - Boronic acid - Boronic acid derivative - Organic metalloid salt - Ether - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aromatic homopolycyclic compound Descrição This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. 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 Certificados(CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Ponto de fusão (°C) 102-106°C Peso molecular 216.040 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 216.096 Da Monoisotopic Mass 216.096 Da Topological Polar Surface Area 49.700 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 222.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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