Neocuproine - ≥98%, used for Neocuproine can be used as ligands: Using Au (I) as catalyst, the aerobic oxidation reaction of benzenol and allyl alcohol was carried out to produce corresponding carbonyl compounds. The aqueous (2, 9-dimethyl-1, 10-o-diazepi

Name: Neocuproine - ≥98%, used for Neocuproine can be used as ligands: Using Au (I) as catalyst, the aerobic oxidation reaction of benzenol and allyl alcohol was carried out to produce corresponding carbonyl compounds. The aqueous (2, 9-dimethyl-1, 10-o-diazepi
SKU: N170560
Availability: InStock

CAS: 484-11-7 Cat. No.: N170560 Fórmula: C₁₄H₁₂N₂ Peso molecular: 208.26 Número CE: 207-601-9

55 Citations COA

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Neocuproine - ≥98% CAS No(484-11-7) by Aladdin Scientific

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Disponível para encomenda

GRADE & PURITY ≥98%

Synonyms

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Specifications Nomes e identificadores Documentation Advanced Data Taxonomic Classification 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 FAQs e artigos Citations of This Product Calculadoras de soluções Revisões

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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice 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.

📚

Literature proof

Cited in 55 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos

Especificações e pureza

≥98%

Aplicação

Neocuproine can be used as ligands: Using Au (I) as catalyst, the aerobic oxidation reaction of benzenol and allyl alcohol was carried out to produce corresponding carbonyl compounds. The aqueous (2, 9-dimethyl-1, 10-o-diazepine)NiCl2 complex can be used

Condições de armazenamento de armazenamento

Store at 2-8°C,Protected from light

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

504753970

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504753970

Sorrisos canónicos

CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C

IUPAC Name

2,9-dimethyl-1,10-phenanthroline

InChIKey

IYRGXJIJGHOCFS-UHFFFAOYSA-N

INCHI

1S/C14H12N2/c1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9/h3-8H,1-2H3

SMILES isoméricas

CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C

WGK Alemanha

CAS alternativo

34302-69-7

Peso molecular

208.26

Reaxy-Rn

153179

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=153179&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

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Classe Phenanthrolines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Classe	Phenanthrolines
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Phenanthrolines
Alternative Parents	Quinolines and derivatives Methylpyridines Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	1,10-phenanthroline - Quinoline - Methylpyridine - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Descrição	This compound belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

Estrutura 3D

Alvos associados (humanos)

CCR1 Tchem C-C chemokine receptor type 1 (1730 Activities)

Discover Target: CCR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR5 Tclin C-C chemokine receptor type 5 (5640 Activities)

Discover Target: CCR5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Data	Item
J2612790	Certificate of Analysis	Sep 20, 2026	N170560
J2612789	Certificate of Analysis	Sep 20, 2026	N170560
J2612787	Certificate of Analysis	Sep 20, 2026	N170560
J2612786	Certificate of Analysis	Sep 20, 2026	N170560
C2604601	Certificate of Analysis	Feb 02, 2026	N170560
C2604616	Certificate of Analysis	Feb 02, 2026	N170560
C2604617	Certificate of Analysis	Feb 02, 2026	N170560
G2616135	Certificate of Analysis	Feb 02, 2026	N170560
K2506028	Certificate of Analysis	Nov 14, 2025	N170560
K2124187	Certificate of Analysis	Sep 04, 2025	N170560
B2108030	Certificate of Analysis	Dec 09, 2024	N170560
I2419617	Certificate of Analysis	Sep 04, 2024	N170560
I2419630	Certificate of Analysis	Sep 04, 2024	N170560
I2419621	Certificate of Analysis	Sep 04, 2024	N170560
I2419620	Certificate of Analysis	Sep 04, 2024	N170560
I2419619	Certificate of Analysis	Sep 04, 2024	N170560
I2419618	Certificate of Analysis	Sep 04, 2024	N170560
A2609010	Certificate of Analysis	Sep 04, 2024	N170560
G2524056	Certificate of Analysis	Sep 04, 2024	N170560
D2526052	Certificate of Analysis	Sep 04, 2024	N170560
I2304099	Certificate of Analysis	Sep 11, 2023	N170560
H2420056	Certificate of Analysis	Sep 11, 2023	N170560
H2414024	Certificate of Analysis	Sep 11, 2023	N170560
J2228123	Certificate of Analysis	Oct 15, 2021	N170560
F2307381	Certificate of Analysis	Oct 15, 2021	N170560
E23291201	Certificate of Analysis	Oct 15, 2021	N170560
L2325016	Certificate of Analysis	Oct 15, 2021	N170560

Solubilidade	Slightly soluble in water and light petroleum. Soluble in methanol, ethanol, acetone, ether and benzene
Sensibilidade	light sensitive
Peso molecular	208.260 g/mol
XLogP3	3.300
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	208.1 Da
Monoisotopic Mass	208.1 Da
Topological Polar Surface Area	25.800 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	227.000
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

Neocuproine - ≥98%, used for Neocuproine can be used as ligands: Using Au (I) as catalyst, the aerobic oxidation reaction of benzenol and allyl alcohol was carried out to produce corresponding carbonyl compounds. The aqueous (2, 9-dimethyl-1, 10-o-diazepi

Storage & shipping

Quality documents

Literature proof

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avaliações dos Clientes

📚 Citations by Application

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