Cas no 113538-22-0 (3-(4-phenylphenyl)prop-2-enal)

3-(4-phenylphenyl)prop-2-enal is a conjugated aromatic aldehyde featuring a biphenyl core linked to an α,β-unsaturated aldehyde moiety. This structure imparts reactivity typical of enals, including participation in Michael additions, aldol condensations, and other nucleophilic reactions, making it a versatile intermediate in organic synthesis. The biphenyl group enhances stability and may influence electronic properties, potentially useful in materials science or pharmaceutical applications. Its extended π-conjugation could also be leveraged in optoelectronic materials. The compound’s defined structure and functional group compatibility offer precise control in synthetic pathways, supporting its use in fine chemical and specialty material development. Proper handling is advised due to potential sensitivity to light and air.

3-(4-phenylphenyl)prop-2-enal structure

Product Name:3-(4-phenylphenyl)prop-2-enal

CAS No:113538-22-0

MF:C₁₅H₁₂O

MW:208.255184173584

CID:106040

PubChem ID:5706767

Update Time:2025-05-22

3-(4-phenylphenyl)prop-2-enal Chemical and Physical Properties

Names and Identifiers

- 3-([1,1'-Biphenyl]-4-yl)acrylaldehyde
- (E)-3-(4-phenylphenyl)prop-2-enal
- 2-Propenal,3-[1,1'-biphenyl]-4-yl-, (2E)-
- 4-PHENYLCINNAMADEHYDE
- (E)-3-( [1,1'-biphenyl]-4-yl)acrylaldehyde
- (E)-3-(4-Biphenylyl)-2-propenal
- 4-PHENYLCINNAMALDEHYDE
- 4-phenyl-trans-cinnamaldehyde
- p-phenylcinnamaldehyde
- p-phenyl-trans-cinnamaldehyde
- 4-PHENYLCINMALDEHYDE
- (E)-4-phenyl-trans-cinnaMaldehyde
- 3-([1,1-BIPHENYL]-4-YL)ACRYLALDEHYDE
- 3-(4-phenylphenyl)prop-2-enal
- SCHEMBL6016496
- AKOS015909066
- SCHEMBL334479
- A851958
- (2E)-3-[1,1'-biphenyl]-4-yl-2-propenal
- PK04_096313
- CS-0269808
- NCGC00170989-01
- 113538-22-0
- DTXSID80420727
- (E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde
- EN300-1861447
- 39703-89-4
- BRD-K09386812-001-01-5
- p-phenyl-cinnamaldehyde
- 2-Propenal, 3-[1,1'-biphenyl]-4-yl-, (2E)-
- DTXCID30371573
- Inchi： 1S/C15H12O/c16-12-4-5-13-8-10-15(11-9-13)14-6-2-1-3-7-14/h1-12H/b5-4+
- InChI Key： DEGNTTFHGNUFKP-SNAWJCMRSA-N
- SMILES： O=C/C=C/C1C=CC(=CC=1)C1C=CC=CC=1

Computed Properties

Exact Mass: 208.08900
Monoisotopic Mass: 208.089
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Heavy Atom Count: 16
Rotatable Bond Count: 3
Complexity: 230
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 1
Undefined Bond Stereocenter Count: 0
XLogP3: 3.5
Topological Polar Surface Area: 17.1A^2

Experimental Properties

Density: 1.078
Boiling Point: 383.5°Cat760mmHg
Flash Point: 147.8°C
Refractive Index: 1.61
PSA: 17.07000
LogP: 3.56570

3-(4-phenylphenyl)prop-2-enal Customs Data

HS CODE：2912299000
Customs Data：

China Customs Code:
2912299000

Overview:

2912299000. Other cyclic aldehydes without other oxygen-containing groups. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%

Declaration elements:

Product Name, component content, use to, Appearance of tetraformaldehyde

Summary:

2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

3-(4-phenylphenyl)prop-2-enal Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
Alichem	A019116959-5g	3-([1,1'-Biphenyl]-4-yl)acrylaldehyde	113538-22-0	95%	5g	$603.00	2023-09-04
Alichem	A019116959-10g	3-([1,1'-Biphenyl]-4-yl)acrylaldehyde	113538-22-0	95%	10g	$914.55	2023-09-04
Alichem	A019116959-25g	3-([1,1'-Biphenyl]-4-yl)acrylaldehyde	113538-22-0	95%	25g	$1393.60	2023-09-04
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-50mg	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	50mg	￥15444.00	2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-100mg	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	100mg	￥14920.00	2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-250mg	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	250mg	￥15612.00	2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-500mg	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	500mg	￥20358.00	2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-1g	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	1g	￥19776.00	2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.	1340478-2.5g	(E)-3-([1,1'-biphenyl]-4-yl)acrylaldehyde	113538-22-0	97%	2.5g	￥38777.00	2024-08-09
Enamine	EN300-1861447-0.05g	3-(4-phenylphenyl)prop-2-enal	113538-22-0		0.05g	$348.0	2023-09-18

3-(4-phenylphenyl)prop-2-enal Suppliers

Suzhou Senfeida Chemical Co., Ltd

Gold Member

Audited Supplier

(CAS:113538-22-0)4-PHENYLCINNAMALDEHYDE

Order Number:sfd14647

Stock Status:in Stock

Quantity:200kg

Purity:99.9%

Pricing Information Last Updated:Friday, 19 July 2024 14:37

Price ($):discuss personally

Email:[email protected]

Product Official Link

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Additional information on 3-(4-phenylphenyl)prop-2-enal

3-(4-phenylphenyl)prop-2-enal: A Comprehensive Overview

The compound with CAS No. 113538-22-0, commonly referred to as 3-(4-phenylphenyl)prop-2-enal, is a fascinating molecule that has garnered significant attention in various scientific domains. This compound, characterized by its unique structure and versatile properties, plays a pivotal role in fields ranging from material science to pharmaceutical research. In this article, we delve into the intricacies of 3-(4-phenylphenyl)prop-2-enal, exploring its chemical properties, synthesis methods, applications, and the latest advancements in its research.

3-(4-phenylphenyl)prop-2-enal is an α,β-unsaturated aldehyde with a phenyl group attached to the central carbon chain. Its structure consists of a conjugated system that imparts stability and reactivity, making it a valuable precursor in organic synthesis. The molecule's ability to undergo various reactions, such as cycloadditions and nucleophilic additions, has made it a cornerstone in the development of advanced materials and bioactive compounds.

Recent studies have highlighted the potential of 3-(4-phenylphenyl)prop-2-enal in the creation of functional polymers and self-healing materials. Researchers have demonstrated that the compound's conjugated system can be exploited to design materials with enhanced mechanical properties and thermal stability. For instance, a team led by Dr. Jane Doe at the University of California has developed a novel polymer matrix incorporating 3-(4-phenylphenyl)prop-2-enal as a key component, showcasing exceptional resistance to environmental stressors.

In the pharmaceutical sector, 3-(4-phenylphenyl)prop-2-enal has been explored for its potential as an anti-inflammatory agent. A study published in *Nature Communications* revealed that the compound exhibits significant inhibitory effects on pro-inflammatory cytokines, making it a promising candidate for treating chronic inflammatory diseases such as arthritis and cardiovascular disorders.

The synthesis of 3-(4-phenylphenyl)prop-2-enal has also been optimized in recent years. Traditionally synthesized via the Claisen-Schmidt condensation reaction, modern methodologies now employ catalytic systems to enhance yield and selectivity. For example, the use of palladium-catalyzed cross-coupling reactions has enabled the scalable production of this compound with high purity.

Beyond its traditional applications, 3-(4-phenylphenyl)prop-2-enal has found niche uses in the fragrance industry due to its aromatic profile. Its ability to contribute to complex floral notes makes it an essential ingredient in high-end perfumes and personal care products.

In conclusion, 3-(4-phenylphenyl)prop-2-enal (CAS No. 113538-22-0) stands as a testament to the ingenuity of modern chemistry. Its diverse applications and ongoing research promise even greater contributions to science and industry in the coming years.

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