15972-55-1
- Product Name:4,4'-(Cyclopenta-2,4-dien-1-ylidenemethylene)bis(methoxybenzene)
- Molecular Formula:C20H18 O2
- Purity:99%
- Molecular Weight:290.362
Product Details;
CasNo: 15972-55-1
Molecular Formula: C20H18 O2
factory and supplier 15972-55-1 4,4'-(Cyclopenta-2,4-dien-1-ylidenemethylene)bis(methoxybenzene) in stock
- Molecular Formula:C20H18 O2
- Molecular Weight:290.362
- Vapor Pressure:7.78E-09mmHg at 25°C
- Refractive Index:1.61
- Boiling Point:477.9°Cat760mmHg
- Flash Point:193.5°C
- PSA:18.46000
- Density:1.127g/cm3
- LogP:4.63170
6,6-Bis(p-methoxyphenyl)fulvene(Cas 15972-55-1) Usage
|
General Description |
6,6-Bis(p-methoxyphenyl)fulvene is a chemical compound with the molecular formula C25H22O2. It is a fulvene derivative that is commonly used in organic synthesis and material science. The compound is a bright yellow solid with a high melting point. It is known for its ability to undergo a variety of organic reactions and can be used as a building block for the synthesis of various organic compounds. Due to its unique structure and reactivity, 6,6-Bis(p-methoxyphenyl)fulvene has potential applications in the development of new materials and the production of pharmaceuticals. |
InChI:InChI=1/C20H18O2/c1-21-18-11-7-16(8-12-18)20(15-5-3-4-6-15)17-9-13-19(22-2)14-10-17/h3-14H,1-2H3
15972-55-1 Relevant articles
Visible-light-induced [4 + 2] cycloaddition of pentafulvenes by organic photoredox catalysis
Asada, Yosuke,Honda, Kiyoshi,Hoshino, Yujiro,Tanaka, Kenta
supporting information, p. 8074 - 8078 (2020/11/03)
We have developed thioxanthylium photore...
Process for producing ethylene/α-olefin copolymer
-
Page/Page column 48; 49, (2018/05/26)
A process capable of producing an ethyle...
Method for producing fulvene
-
Paragraph 0039, (2017/03/08)
PROBLEM TO BE SOLVED: To provide a metho...
An improved pathway to 6,6-disubstituted fulvenes
Chajara, Khalil,Ottosson, Henrik
, p. 6741 - 6744 (2007/10/03)
Pentafulvenes with alkyl and/or aryl sub...
15972-55-1 Process route
-
-
90-96-0
bis(p-methoxyphenyl)methanone
-
-
542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene
-
-
15972-55-1
6,6-bis(4-methoxyphenyl)fulvene
| Conditions | Yield |
|---|---|
|
bis(p-methoxyphenyl)methanone;
With
aluminum (III) chloride;
In
tetrahydrofuran;
at 20 ℃;
for 1h;
Inert atmosphere;
cyclopenta-1,3-diene;
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at 20 ℃;
for 1h;
Inert atmosphere;
Schlenk technique;
|
93% |
|
With
sodium;
In
ethanol;
Heating;
|
10% |
|
cyclopenta-1,3-diene;
With
sodium hydride;
In
tetrahydrofuran;
at 0 ℃;
for 1h;
bis(p-methoxyphenyl)methanone;
In
tetrahydrofuran;
at 0 - 20 ℃;
|
6% |
|
With
sodium methylate;
|
|
|
With
sodium methylate;
In
tetrahydrofuran; methanol;
|
|
|
With
sodium methylate;
In
tetrahydrofuran;
at 50 ℃;
for 12h;
|
|
|
With
methanol; sodium;
In
tetrahydrofuran;
|
-
-
90-96-0
bis(p-methoxyphenyl)methanone
-
-
lithium cyclopentadienide
-
-
15972-55-1
6,6-bis(4-methoxyphenyl)fulvene
| Conditions | Yield |
|---|---|
|
lithium cyclopentadienide;
With
1,3-dimethyl-2-imidazolidinone;
In
tetrahydrofuran;
at 20 ℃;
for 0.5h;
Inert atmosphere;
Cooling with ice;
bis(p-methoxyphenyl)methanone;
In
tetrahydrofuran;
for 1h;
Reflux;
|
30.7% |
15972-55-1 Upstream products
-
90-96-0
bis(p-methoxyphenyl)methanone
-
542-92-7
cyclopenta-1,3-diene
-
135655-33-3
bis(4-methoxyphenyl)selenoketone
-
958-80-5
bis(4-methoxyphenyl)thione
15972-55-1 Downstream products
-
54705-60-1
4,9-dibenzoyl-1-(4,4'-dimethoxy-benzhydrylidene)-3a,4,9,9a-tetrahydro-1H-cyclopenta[b]quinoxaline
-
67944-88-1
1-(4,4'-dimethoxy-benzhydrylidene)-4,9-bis-(4-nitro-benzoyl)-3a,4,9,9a-tetrahydro-1H-cyclopenta[b]quinoxaline
-
77978-39-3
4-(4,4'-Dimethoxybenzhydryliden)-2-methyl-1,3-diphenyl-4H-cyclopenta
pyrrol -
77978-40-6
3,3'-(4,4'-Dimethoxybenzhydrylidenmethylen)bis<1-methyl-2,5-diphenylpyrrol>
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