1H-Naphth[2,3-d]imidazole(8CI,9CI)

Base Information

Chemical Name:1H-Naphth[2,3-d]imidazole(8CI,9CI)
CAS No.:269-07-8
Molecular Formula:C11H8 N2
Molecular Weight:168.198
Hs Code.:
Mol file:269-07-8.mol

Synonyms:Naphth[2,3-d]imidazole(6CI); 1,3-Diaza-1H-benz[f]indene; Naphtho[2,3-d]imidazole

Suppliers and Price of 1H-Naphth[2,3-d]imidazole(8CI,9CI)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1H-NAPHTHO[2,3-D]IMIDAZOLE 95.00%
5MG
$ 495.96

Total 5 raw suppliers

Chemical Property of 1H-Naphth[2,3-d]imidazole(8CI,9CI)

Chemical Property:

Vapor Pressure:2.59E-08mmHg at 25°C
Melting Point:220 °C(Solv: water (7732-18-5); methanol (67-56-1))
Boiling Point:463.1°Cat760mmHg
PKA:12.54±0.10(Predicted)
Flash Point:275.4°C
PSA：28.68000
Density:1.301g/cm³
LogP:2.71610

Purity/Quality:

99% ^*data from raw suppliers

1H-NAPHTHO[2,3-D]IMIDAZOLE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

General Description 1H-Naphth[2,3-d]imidazole is a polycyclic aromatic heterocycle that serves as a key structural motif in various applications, including catalytic synthesis, fluorescent probes, and nucleoside analogue design. It exhibits Lewis acid catalytic activity in metal-organic frameworks (MOFs) for naphthimidazole synthesis, demonstrating excellent yield without pre-activation. Additionally, its derivatives function as ratiometric fluorescent probes for fluoride ions, leveraging hydrogen bonding interactions for selective detection. 1H-Naphth[2,3-d]imidazole(8CI,9CI) is also utilized in designing nucleoside analogues for detecting mutagenic DNA adducts like O⁶-methylguanine, highlighting its role in biosensing. Furthermore, naphthoimidazolium-based probes enable two-photon microscopy imaging of hypochlorous acid in cellular environments, emphasizing its versatility in chemical and biological research.

Technology Process of 1H-Naphth[2,3-d]imidazole(8CI,9CI)

There total 9 articles about 1H-Naphth[2,3-d]imidazole(8CI,9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 771-97-1
2,3-Diaminonaphthalene

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 269-07-8
naphtho[2,3-d]imidazole

Guidance literature:: With {[Zn(3,5-bis(4-oxo-4H-pyridin-1-yl)benzoate)Cl]*5H₂O}_n; at 120 ℃; for 48h; under 760.051 Torr; Reagent/catalyst; Temperature; Catalytic behavior;
DOI:10.1016/j.poly.2020.114584

Reference yield: 87.0%

: 269-07-8
naphtho[2,3-d]imidazole

Guidance literature:: With Imidazole hydrochloride; at 120 ℃; for 6h;

Reference yield: 83.0%

: 124-38-9,18923-20-1
carbon dioxide

: 771-97-1
2,3-Diaminonaphthalene

: 269-07-8
naphtho[2,3-d]imidazole

Guidance literature:: With diphenylsilane; C₃₃H₃₆BO₆^(3-)*Eu⁽³⁺⁾*H₂O*2C₃H₇NO; In acetonitrile; at 120 ℃; for 24h; under 7500.75 Torr; Autoclave;
DOI:10.1002/anie.201901171