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2-Phenylquinoline

CAS No.
612-96-4
Chemical Name:
2-Phenylquinoline
Synonyms
830g;2-Phenylquinoline;a-Phenylquinoline;Phenylquinoline,99%;2-Phenylquinoline>Phenylquinoline, 99%;Quinoline, 2-phenyl-;2-Phenylquinoline 99%;alpha-Phenylquinoline;2-Phenylquinoline, 99+%
CBNumber:
CB7408748
Molecular Formula:
C15H11N
Molecular Weight:
205.25
MDL Number:
MFCD00011568
MOL File:
612-96-4.mol
MSDS File:
SDS
Last updated:2024-01-05 11:48:35

2-Phenylquinoline Properties

Melting point 84-85 °C (lit.)
Boiling point 363 °C
Density 1.1155 (rough estimate)
refractive index 1.6550 (estimate)
storage temp. Sealed in dry,Room Temperature
pka 4.52±0.10(Predicted)
form Crystalline Powder
color White to light yellow
Water Solubility SLIGHTLY SOLUBLE
λmax 258nm(lit.)
CAS DataBase Reference 612-96-4(CAS DataBase Reference)
NIST Chemistry Reference Quinoline, 2-phenyl-(612-96-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
HS Code  29334900
NFPA 704
0
1 0

2-Phenylquinoline price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 299650 2-Phenylquinoline 99% 612-96-4 1g $80.9 2024-03-01 Buy
Sigma-Aldrich 299650 2-Phenylquinoline 99% 612-96-4 5g $384 2024-03-01 Buy
TCI Chemical P2057 2-Phenylquinoline >98.0%(GC)(T) 612-96-4 1g $66 2024-03-01 Buy
TCI Chemical P2057 2-Phenylquinoline >98.0%(GC)(T) 612-96-4 5g $223 2024-03-01 Buy
Alfa Aesar H31920 2-Phenylquinoline, 99+% 612-96-4 1g $70.65 2024-03-01 Buy
Product number Packaging Price Buy
299650 1g $80.9 Buy
299650 5g $384 Buy
P2057 1g $66 Buy
P2057 5g $223 Buy
H31920 1g $70.65 Buy

2-Phenylquinoline Chemical Properties,Uses,Production

Description

2-Phenylquinoline is the major quinoline alkaloid of Galipea iongiflora, a Bolivian plant used as treatment for cutaneous leishmaniasis. Antinociceptive properties of 2-phenylquinoline isolated from the bark of Galipea iongiflora against different models of pain in mice were evaluated.

Chemical Properties

white to light yellow crystalline powder

Uses

2-Phenylquinoline was used in quantitative structure-activity relationship (QSAR) analyses of estrogen receptor β-selective ligands.

Preparation

Synthesis of 2-phenylquinoline: Quinoline (1.0 g, 7.742 mmol) and phenyl lithium (2.30 mL, 2 M, 23.22 mmol) were reacted according to general procedure. Purification of the residue by silica gel column chromatography (EtOAc:MeOH:Et3N; 10-30:1:1 or PhMe:MeOH:Et3N; 10:1:1) gave 2-phenylquinoline (0.66 g, 42%) as an orange solid.
Aniline (0.140 g, 1.50 mmol) and cinnamaldehyde (0.132 g, 1.00 mmol) were dissolved in toluene in a reaction vial equipped with a magnetic stirrer bar, followed by the addition of K10 (0.50 g). The reaction mixture was heated at a temperature of 110 ?C for 3 hours. After completion of the reaction, the crude product was purified by column chromatography over silica gel eluting with a mixture of Hexane : Ethyl acetate (20:1) to produce 2-Phenylquinoline as a yellow solid (0.044 g, 21%); (m.p. 82-84 ?C) (lit. 84-85 °C); Rf 0.67 (20:1 hexane:ethyl acetate);
1H NMR (400 MHz, CDCl3) δH 7.46-7.51 (1H, m, H-4’), 7.53-7.56 (3H, m, H-6, 3’, 5’), 7.73- 7.77 (1H, m, H-7), 7.85 (1H, d, J = 8.31 Hz, H-5), 7.88-7.91 (1H, d, J = 8.31 Hz, H-3), 8.18- 8.27 (4H, m, H-4, 8, 2’, 6’)
13C NMR(400 MHz, CDCl3) δC 119.2 (C-3), 126.7 (C-6), 127.2 (C-4a), 127.5 (C-2’, 6’), 127.9 (C-5), 128.4 (C-3’, 5’), 128.7 (C-4’), 128.9 (C-7, 8), 129.8 (C-4), 130.3 (C-1’), 137.9 (C-8a), 157.2 (C-2)

Synthesis Reference(s)

Synthetic Communications, 23, p. 1959, 1993 DOI: 10.1080/00397919308009854
Chemical and Pharmaceutical Bulletin, 26, p. 3485, 1978 DOI: 10.1248/cpb.26.3485
Journal of the American Chemical Society, 71, p. 2327, 1949 DOI: 10.1021/ja01175a017

2-Phenylquinoline Preparation Products And Raw materials

Global( 199)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 7786 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15928 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10248 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81148696 +8615536356810 1047@dideu.com China 3459 58

View Lastest Price from 2-Phenylquinoline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Phenylquinoline pictures 2024-01-06 2-Phenylquinoline
612-96-4
US $188.00-1.00 / KG 1KG 99%, 99.5% Sublimated g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
2-Phenylquinoline  pictures 2022-03-07 2-Phenylquinoline
612-96-4
US $1.10 / g 1g 99.00% 100 Tons Dideu Industries Group Limited
2-Phenylquinoline pictures 2020-04-30 2-Phenylquinoline
612-96-4
US $0.10 / KG 1KG 99.0% 1000 tons Shaanxi Dideu Medichem Co. Ltd
  • 2-Phenylquinoline pictures
  • 2-Phenylquinoline
    612-96-4
  • US $188.00-1.00 / KG
  • 99%, 99.5% Sublimated
  • Henan Fengda Chemical Co., Ltd
alpha-Phenylquinoline 2-Phenylquinoline, 99+% Phenylquinoline,99% a-Phenylquinoline 2-Phenylquinoline Phenylquinoline, 99% 2-Phenylquinoline 99% 2-Phenylquinoline, 99+% 1GR 2-Phenylquinoline> 830g Quinoline, 2-phenyl- 2-Phenylquinoline ISO 9001:2015 REACH 612-96-4 C6H5C9H6N C15H11N Building Blocks Quinolines Heterocyclic Building Blocks Heterocyclic Building Blocks Quinolines Building Blocks Quinolines, Quinazolines and derivatives API intermediates