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9-VINYLANTHRACENE

CAS No.
2444-68-0
Chemical Name:
9-VINYLANTHRACENE
Synonyms
Anthracene, 9-ethenyl-;9-Ethenyl anthracene;9-VINYLANTHRACENE;9-Ethenylanthracen;10-vinylanthracene;9-Vinylanthracene,97%;9-Vinylanthracene 97%;9-vinyl-anthracene radical cation
CBNumber:
CB9248029
Molecular Formula:
C16H12
Molecular Weight:
204.27
MDL Number:
MFCD00003576
MOL File:
2444-68-0.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:48

9-VINYLANTHRACENE Properties

Melting point 62-65 °C (lit.)
Boiling point 61-66 °C/10 mmHg (lit.)
Density 1.1570 (estimate)
refractive index 1.5000 (estimate)
Flash point 61-66°C/10mm
storage temp. Store below +30°C.
form powder to crystal
color White to Yellow to Orange
BRN 2041641
InChI InChI=1S/C16H12/c1-2-14-15-9-5-3-7-12(15)11-13-8-4-6-10-16(13)14/h2-11H,1H2
InChIKey OGOYZCQQQFAGRI-UHFFFAOYSA-N
SMILES C1=C2C(C=C3C(=C2C=C)C=CC=C3)=CC=C1
CAS DataBase Reference 2444-68-0(CAS DataBase Reference)
FDA UNII A3692NGE8J
UNSPSC Code 12352005

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Safety Statements  22-24/25
WGK Germany  3
HS Code  2902 90 00
NFPA 704
1
0 0

9-VINYLANTHRACENE price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.24593 9-Vinylanthracene for synthesis 2444-68-0 0.5g $97.7 2024-03-01 Buy
Sigma-Aldrich V1708 9-Vinylanthracene 97% 2444-68-0 1g $128 2023-06-20 Buy
Sigma-Aldrich V1708 9-Vinylanthracene 97% 2444-68-0 5g $404 2023-06-20 Buy
TCI Chemical V0130 9-Vinylanthracene 2444-68-0 1G $63 2025-07-31 Buy
TCI Chemical V0130 9-Vinylanthracene 2444-68-0 5G $184 2025-07-31 Buy
Product number Packaging Price Buy
8.24593 0.5g $97.7 Buy
V1708 1g $128 Buy
V1708 5g $404 Buy
V0130 1G $63 Buy
V0130 5G $184 Buy

9-VINYLANTHRACENE Chemical Properties,Uses,Production

Chemical Properties

yellow to green crystalline solid

Uses

9-Vinylanthracene (cas# 2444-68-0) is a compound useful in organic synthesis.

Synthesis Reference(s)

The Journal of Organic Chemistry, 56, p. 4035, 1991 DOI: 10.1021/jo00012a043
Synthesis, p. 319, 1981

Synthesis

9-Anthraldehyde

642-31-9

Iodomethane

74-88-4

9-VINYLANTHRACENE

2444-68-0

General method C: Preparation of compounds A17-A24 by catalytic Wittig reaction. catalyst Aid (0.2 mmol, 20 mol%) and base A2 (2.0-3.5 mmol, 2.0-3.5 eq.) were added to a 1-dram vial fitted with a stirrer in air. If a solid aldehyde (1.0-1.2 mmol, 1.0-1.2 eq.) is used, it is added together at this point. The vial is then sealed with a septum and the air in the vial is replaced with argon. Toluene (1.4 mL) and the liquid reagents: aldehydes (1.2 mmol, 1.2 eq.) and organic halides (1.0 mmol, 1.0 eq.) were added sequentially. Diphenylsilane (1.2 mmol, 1.2 eq.) was then added and the septum was replaced with a PTFE-lined screw cap under an inert atmosphere. The reaction mixture was heated at 140°C or 150°C for 24-48 hours. After the reaction has been carried out for 24 hours, the base and halide are added additionally and the reaction is continued up to 48 hours. After completion of the reaction, the crude product was filtered through Celite, concentrated under reduced pressure and finally purified by fast column chromatography. Synthesis of 9-vinylanthracene (A23): In toluene (0.7 mL), 9-anthracenecarboxaldehyde (128 mg, 0.6 mmol, 1.2 eq.), iodomethane (31 μL, 0.5 mmol, 1.0 eq.), and diphenylsilane (112 μL, 0.6 mmol, 1.2 eq.) were added to the reaction with catalyst A3b (30 mg, 20 mol%) and base A2 (210 mg, 1.5 mmol, 3.0 eq.) were added, and the reaction was carried out at 140 °C for 24 hours. During the reaction, iodomethane and A2 were added twice at 0 h and 4 h. The crude product was purified by fast column chromatography (eluent: hexane, Rf = 0.35) to afford 9-vinylanthracene (A23, 66 mg, 65% yield) in yellow liquid form.1H NMR (400 MHz, CDCl3) δ: 5.68 (d, J = 18.0 Hz, 1H), 6.06 (d, J = 18.0 Hz, 1H), 6.06 (d, J = 18.0 Hz, 1H) 6.06 (d, J = 11.5 Hz, 1H), 7.48-7.60 (m, 5H), 8.00-8.08 (m, 2H), 8.35-8.40 (m, 2H).

Purification Methods

Purify it by vacuum sublimation. It has also been purified by chromatography on silica gel with cyclohexane as eluent, and recrystallised from EtOH [Werst et al. J Am Chem Soc 109 32 1987]. [Beilstein 5 IV 2415.]

References

[1] Angewandte Chemie - International Edition, 2014, vol. 53, # 47, p. 12907 - 12911
[2] Angew. Chem., 2014, vol. 126, # 47, p. 13121 - 13125,5
[3] Patent: WO2014/140353, 2014, A1. Location in patent: Page/Page column 59; 68; 69; 70

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View Lastest Price from 9-VINYLANTHRACENE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
9-VINYLANTHRACENE pictures 2025-08-08 9-VINYLANTHRACENE
2444-68-0
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mujin Biotechnology Co.,Ltd
9-VINYLANTHRACENE pictures 2025-06-27 9-VINYLANTHRACENE
2444-68-0
US $0.00 / KG 1KG 99% 500000kg Hebei Chuanghai Biotechnology Co., Ltd
9-VINYLANTHRACENE pictures 2025-06-20 9-VINYLANTHRACENE
2444-68-0
US $20.00-1.00 / kg 1kg 0.99 20 tons Hebei Yanxi Chemical Co., Ltd.
9-Ethenyl anthracene 9-VINYLANTHRACENE 10-vinylanthracene 9-Ethenylanthracen 9-Vinylanthracene 97% 9-Vinylanthracene,97% Anthracene, 9-ethenyl- 9-vinyl-anthracene radical cation 2444-68-0 ALKENE Organic Building Blocks Alkenes Acyclic Building Blocks Styrenes Photoluminescent Materials > Fluorescent MonomersPolymer Science Monomers Photonic and Optical Materials Styrene and Functionalized Styrene MonomersPolymer Science Vinyl Halides, Amines, Amides, and Other Vinyl Monomers