Cas no 1203-68-5 (2-Phenylbenzaldehyde)
2-Phenylbenzaldehyde Chemical and Physical Properties
Names and Identifiers
-
- 2-Phenylbenzaldehyde
- Biphenyl-2-carbaldehyde
- Biphenyl-2-carboxaldehyde
- 2-Biphenylcarboxaldehyde
- 2-Formyl-1,1'-biphenyl
- AKOS005216888
- 2-FORMYL-BIPHENYL
- J-510257
- SY003223
- biphenyl formaldehyde
- Z727783562
- 2-Difenilaldeide [Italian]
- 1203-68-5
- [1,1'-Biphenyl]carboxaldehyde
- FT-0633478
- 2-phenyl-benzaldehyde
- CS-W002824
- biphenylaldehyde
- (1,1'-Biphenyl)-2-carboxaldehyde
- biphenyl aldehyde
- biphenyl-2 -aldehyde
- EN300-51583
- 2-Biphenylcarbaldehyde
- (1,1'-Biphenyl)carboxaldehyde
- biphenyl carboxaldehyde
- SCHEMBL96494
- BB 0255005
- 2-Difenilaldeide
- 55171-99-8
- [1,1'-Biphenyl]-2-carboxaldehyde
- (1,1-biphenyl)-2-carboxaldehyde;2-difenilaldeide
- 2,7-NAPHTHALENEDISULFONYLCHLORIDE
- A25933
- MFCD01740431
- BRN 2081880
- CHEMBL124879
- AC-18698
- 2-formylbiphenyl
- PS-8524
- Biphenyl-2-carboxaldehyde, 96%
- DTXSID80923309
- Biphenylcarboxaldehyde
- [1,1'-biphenyl]-2-carbaldehyde
- biphenyl-2-aldehyde
- LCRCBXLHWTVPEQ-UHFFFAOYSA-N
- DB-021493
-
- MDL: MFCD01740431
- Inchi: 1S/C13H10O/c14-10-12-8-4-5-9-13(12)11-6-2-1-3-7-11/h1-10H
- InChI Key: LCRCBXLHWTVPEQ-UHFFFAOYSA-N
- SMILES: O=CC1C=CC=CC=1C1C=CC=CC=1
Computed Properties
- Exact Mass: 182.07300
- Monoisotopic Mass: 182.073164938g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 182
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 17.1?2
Experimental Properties
- Color/Form: Liquid
- Density: 1.130?g/mL?at 25?°C(lit.)
- Boiling Point: 91-92?°C/0.15?mmHg(lit.)
- Flash Point: Fahrenheit: 215.6 ° f < br / > Celsius: 102 ° C < br / >
- Refractive Index: n20/D >1.6220(lit.)
- PSA: 17.07000
- LogP: 3.16610
- Solubility: Not determined
2-Phenylbenzaldehyde Security Information
-
Symbol:
- Signal Word:Warning
- Hazard Statement: H315,H319,H335
- Warning Statement: P261,P305+P351+P338
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26-S36
- RTECS:DV1771000
-
Hazardous Material Identification:
- Safety Term:S26;S36
- Storage Condition:2-8°C
- Risk Phrases:R36/37/38
2-Phenylbenzaldehyde Customs Data
- HS CODE:2912299000
- Customs Data:
China Customs Code:
2912299000Overview:
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%
2-Phenylbenzaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 208224-1g |
2-Biphenylcarboxaldehyde |
1203-68-5 | 95% | 1g |
£12.00 | 2022-03-01 | |
| Fluorochem | 208224-5g |
2-Biphenylcarboxaldehyde |
1203-68-5 | 95% | 5g |
£51.00 | 2022-03-01 | |
| Fluorochem | 208224-10g |
2-Biphenylcarboxaldehyde |
1203-68-5 | 95% | 10g |
£82.00 | 2022-03-01 | |
| Fluorochem | 208224-25g |
2-Biphenylcarboxaldehyde |
1203-68-5 | 95% | 25g |
£149.00 | 2022-03-01 | |
| Fluorochem | 208224-100g |
2-Biphenylcarboxaldehyde |
1203-68-5 | 95% | 100g |
£379.00 | 2022-03-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B122426-1g |
2-Phenylbenzaldehyde |
1203-68-5 | 96% | 1g |
¥58.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B122426-5g |
2-Phenylbenzaldehyde |
1203-68-5 | 96% | 5g |
¥224.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B122426-25g |
2-Phenylbenzaldehyde |
1203-68-5 | 96% | 25g |
¥896.90 | 2023-09-04 | |
| AstaTech | 61416-1/G |
2-FORMYL-BIPHENYL |
1203-68-5 | 97% | 1g |
$30 | 2023-09-16 | |
| AstaTech | 61416-5/G |
2-FORMYL-BIPHENYL |
1203-68-5 | 97% | 5g |
$48 | 2023-09-16 |
2-Phenylbenzaldehyde Suppliers
2-Phenylbenzaldehyde Related Literature
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
-
Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
-
Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
-
Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
-
Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
Additional information on 2-Phenylbenzaldehyde
2-Phenylbenzaldehyde: A Comprehensive Overview
2-Phenylbenzaldehyde, also known by its CAS number 1203-68-5, is a fascinating organic compound with a rich history and diverse applications. This compound, which belongs to the class of aromatic aldehydes, has been the subject of extensive research due to its unique chemical properties and potential uses in various industries. In this article, we will delve into the structural characteristics, chemical properties, applications, and recent advancements related to 2-Phenylbenzaldehyde.
The molecular structure of 2-Phenylbenzaldehyde consists of a benzene ring substituted with a phenyl group at the second position and an aldehyde group at the first position. This arrangement imparts the compound with distinct electronic and steric properties, making it highly reactive in certain chemical transformations. Recent studies have highlighted the importance of these structural features in determining the compound's reactivity and selectivity in various reactions.
Chemical Properties
2-Phenylbenzaldehyde exhibits several notable chemical properties that make it valuable in both academic and industrial settings. For instance, its aldehyde group renders it susceptible to nucleophilic addition reactions, a property that has been exploited in the synthesis of various organic compounds. Additionally, the compound's aromaticity contributes to its stability and ability to undergo electrophilic substitution reactions. Recent research has focused on optimizing these reactions to enhance yield and selectivity.
Applications
The applications of 2-Phenylbenzaldehyde span across multiple domains, including pharmaceuticals, agrochemicals, and materials science. In the pharmaceutical industry, it serves as an intermediate in the synthesis of bioactive compounds with potential therapeutic applications. For example, studies have shown that derivatives of 2-Phenylbenzaldehyde exhibit anti-inflammatory and antioxidant activities, making them promising candidates for drug development.
In agrochemicals, 2-Phenylbenzaldehyde finds use as a precursor in the synthesis of pesticides and herbicides. Its ability to undergo various chemical transformations allows for the creation of compounds with enhanced efficacy and reduced environmental impact. Recent advancements in green chemistry have further expanded its utility in sustainable agricultural practices.
Synthesis and Production
The synthesis of 2-Phenylbenzaldehyde typically involves either oxidation of the corresponding alcohol or direct coupling reactions. One widely used method is the oxidation of 2-phenylethanol using oxidizing agents like potassium permanganate or chromium-based reagents. Recent studies have explored alternative oxidation methods that are more environmentally friendly and efficient.
Safety Considerations
Although generally considered non-toxic under normal handling conditions,1203-68-5 (2-Phenylbenzaldehyde) Related Products
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