- CasNo 4425-73-4
- Purity 99%
Cost-effective and customizable 9-FLUORENYLIDENEACETIC ACID 4425-73-4 for sale
- Molecular Formula: C15H9O2-
- Molecular Weight: 222.243
- Vapor Pressure: 1.22E-06mmHg at 25°C
- Melting Point: 231-233oC
- Boiling Point: 385.7°Cat760mmHg
- Flash Point: 284.1°C
- PSA： 37.30000
- Density: 1.387g/cm3
- LogP: 3.18330
9-FLUORENYLIDENEACETIC ACID(Cas 4425-73-4) Usage
|
General Description |
9-FLUORENYLIDENEACETIC ACID is a chemical compound with the molecular formula C15H12O2. It is often used in organic synthesis, and it is known for its ability to facilitate the formation of peptide bonds in peptide synthesis. 9-FLUORENYLIDENEACETIC ACID has also been studied for its potential use as a plant growth regulator, with research indicating that it may have the ability to promote the growth and development of various plants. Additionally, 9-FLUORENYLIDENEACETIC ACID has been investigated for its potential anti-inflammatory and anti-cancer properties, making it a subject of interest in medicinal chemistry research. Overall, 9-FLUORENYLIDENEACETIC ACID is a versatile compound with various potential applications in both chemical synthesis and biological studies. |
InChI:InChI=1/C15H10O2/c16-15(17)9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-9H,(H,16,17)/p-1
4425-73-4 Relevant articles
UREA DERIVATIVES USEFUL AS CALCIUM RECEPTOR MODULATORS
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Page/Page column 140-142, (2008/06/13)
The present invention provides compounds...
UREA DERIVATIVES METHODS FOR THEIR MANUFACTURE AND USES THEREOF
-
Page/Page column 66, (2010/11/24)
The present invention provides compounds...
A CONVENIENT PREPARATION OF 9H-FLUORENE-9-ACETIC ACID
Goehring, R. Richard
, p. 476 - 478 (2007/10/02)
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Reaction of Olefins with Malonamide in the Presence of Manganese(III) Acetate. Formation of α,β-Unsaturated γ-Lactones and γ-Lactams
Nishino, Hiroshi
, p. 217 - 222 (2007/10/02)
The reaction of olefins with malonamide ...
4425-73-4 Process route
-
-
27973-36-0
dibenzofulvenecarboxylic acid ethyl ester
-
-
4425-73-4
fluoren-9-ylidene-acetic acid
Conditions
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide; ethanol; water;
at 60 ℃;
for 0.75h;
|
99%
|
|
dibenzofulvenecarboxylic acid ethyl ester;
With
sodium hydroxide; water;
In
ethanol;
at 60 ℃;
for 0.75h;
In
water; ethyl acetate;
pH=3;
|
99%
|
|
(hydrolysis);
|
|
|
With
sodium hydroxide;
|
|
|
With
sodium hydroxide;
In
ethanol;
Heating;
|
|
|
Multi-step reaction
with
3
steps
1: Br2
2: Et3
N
3: KOtBu
With
potassium tert-butylate; bromine; triethylamine;
|
|
|
Multi-step reaction
with
4
steps
1: Br2
2: Et3
N
3: aq. KOH / ethanol
4: KOEt
With
potassium hydroxide; potassium ethoxide; bromine; triethylamine;
In
ethanol;
|
-
-
4425-71-2
2-(9H-fluoren-9-ylidene)acetaldehyde
-
-
4425-73-4
fluoren-9-ylidene-acetic acid
Conditions
| Conditions | Yield |
|---|---|
|
With
silver(l) oxide;
|
4425-73-4 Upstream products
-
486-25-9
9-fluorenone
-
4425-71-2
2-(9H-fluoren-9-ylidene)acetaldehyde
-
872280-79-0
ethyl 2-(9H-fluoren-9-yl)-2-hydroxyacetate
-
141-52-6
sodium ethanolate
4425-73-4 Downstream products
-
146967-87-5
methyl 2-(9H-fluoren-9-ylidene)acetate
-
4612-64-0
9-(bromomethylene)-9H-fluorene
-
65779-23-9
3-{4-[2-(2-Fluoren-9-ylidene-acetylamino)-ethyl]-phenyl}-propionic acid ethyl ester
-
19656-55-4
2-Phenyl-3.3-(o-biphenylen)-bernsteinsaeure
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