p-Fluoro benzaldehyde - ≥98% , CAS No.459-57-4

CAS: 459-57-4 Cat. No.: F109178 Peso molecular: 124.11 Beilstein Registry Number: 385857 Número EC: 207-293-6
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
4-fluoro benzaldehyde | N8681893GA | FT-0618504 | STK801571 | CAS-459-57-4 | InChI=1/C7H5FO/c8-7-3-1-6(5-9)2-4-7/h1-5 | AKOS000118950 | 4-flouro benzaldehyde | 4fluorobenzaldehyde | 4-Fluorobenzaldehyde | 4-fluoro-benzaldehy-de | 4-fluorobenz-aldehyde | W
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
F109178-25g
5
9,90US$
100g
F109178-100g
4
20,90US$
500g
F109178-500g
3
83,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 28 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Usually used in the preparation of pyrazolopyridine UR-13756.

Specifications

Sinónimos
4-fluoro benzaldehyde | N8681893GA | FT-0618504 | STK801571 | CAS-459-57-4 | InChI=1/C7H5FO/c8-7-3-1-6(5-9)2-4-7/h1-5 | AKOS000118950 | 4-flouro benzaldehyde | 4fluorobenzaldehyde | 4-Fluorobenzaldehyde | 4-fluoro-benzaldehy-de | 4-fluorobenz-aldehyde | W
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488184072
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184072
Sonrisas canónicasC1=CC(=CC=C1C=O)F
IUPAC Name4-fluorobenzaldehyde
InChIKeyUOQXIWFBQSVDPP-UHFFFAOYSA-N
INCHI1S/C7H5FO/c8-7-3-1-6(5-9)2-4-7/h1-5H
Isómeros SMILES C1=CC(=CC=C1C=O)F
WGK Alemania 2
Número ONU 1989
Peso molecular 124.11
Beilstein 385857
Reaxy-Rn 385857
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=385857&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassBenzoyl derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoyl derivatives
Alternative Parents Benzaldehydes  Fluorobenzenes  Aryl fluorides  Organofluorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzoyl - Benzaldehyde - Aryl-aldehyde - Halobenzene - Fluorobenzene - Aryl halide - Aryl fluoride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Aldehyde - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
SLC6A1 Tclin GABA transporter 1 (308 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
B16-F10 (4610 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

17 results found

Lot NumberCertificate TypeFechaArticulo
J2217497Certificate of AnalysisApr 03, 2026 F109178
H2020111Certificate of AnalysisDec 22, 2025 F109178
D2312277Certificate of AnalysisJan 15, 2025 F109178
D2411453Certificate of AnalysisMar 23, 2024 F109178
D2411454Certificate of AnalysisMar 23, 2024 F109178
A2423218Certificate of AnalysisJan 26, 2024 F109178
A2423219Certificate of AnalysisJan 26, 2024 F109178
A2423220Certificate of AnalysisJan 26, 2024 F109178
B2626132Certificate of AnalysisJan 26, 2024 F109178
H2512059Certificate of AnalysisJan 26, 2024 F109178
A2405038Certificate of AnalysisJan 12, 2024 F109178
F2104320Certificate of AnalysisMar 10, 2023 F109178
F2104319Certificate of AnalysisMar 10, 2023 F109178
F2104321Certificate of AnalysisMar 10, 2023 F109178
J2217494Certificate of AnalysisSep 15, 2022 F109178
J2217610Certificate of AnalysisSep 15, 2022 F109178
H2020113Certificate of AnalysisJun 17, 2022 F109178

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Propiedades químicas y físicas
Sensibilidadair sensitive
Índice de refracción1.52
Punto de inflamación (°F)132.8 °F
Punto de inflamación (°C)56℃
Punto de ebullición (°C)179-181°C
Punto de fusión (°C)-10°C
Peso molecular124.110 g/mol
XLogP31.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass124.032 Da
Monoisotopic Mass124.032 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count9
Formal Charge0
Complexity95.100
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Qiushuang Li, Bing Zhao, Xiangdong Kong, Liyan Wang, Wei Kan, Bo Song, Rui Yu, Pengfei Zhang.  (2023)  Multi-responsive fluorescent covalent organic framework based on phenanthro[9,10-d]imidazole moiety for relayed detection of Cu2+/Al3+ followed by PO43− and its applications.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2023.111886]
2. Yuqin Wei, Long Zhao, Yongdi Liang, Mingcai Yuan, Qijie Wu, Zhaoli Xue, Xinping Qiu, Jianming Zhang.  (2023)  Enhanced cobalt porphyrin-catalytic oxygen reduction reactions by introducing benzoyloxy substitutes.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.146575]
3. Shi Zhou, Yiting Zhu, Haoran Hu, Chenghan Li, Jie Jiang, Jianyu Huang, Biao Zhang.  (2023)  Tuning the LiF content in the SEI by engineering the molecular structures of porous organic polymers for solid-state lithium metal batteries.  Journal of Materials Chemistry A,  11  (11): (5636-5644).  [PMID:] [10.1039/D2TA09896B]
4. Siyuan Chang, Sen Zhang, Tianyi Chen, Lei Xu, Sumin Ge, Bingfeng Li, Chenke Yun, Guoxin Zhang, Xuejun He, Xin Pan.  (2023)  Efficient synthesis of 5-hydroxymethyl-2-furancarboxylic acid from bio-based high-concentration 5-hydroxymethylfurfural via highly tolerant aldehyde dehydrogenase.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2023.112966]
5. Shuang-Qiang Liu, Zhi-Chen Mao, Yan-Li Xu, Xiao-Man Chen, Hui-Ling Wang, Qi Wang, Jian-Hua Wei, Ri-Zhen Huang, Ye Zhang.  (2022)  Discovery of two biotin-PEG4‑diarylidenyl piperidone prodrugs as potent antitumor agents with good efficacy, limited toxicity, and low resistance.  BIOORGANIC CHEMISTRY,      [PMID:36538834] [10.1016/j.bioorg.2022.106323]
6. Xiaoqing Yuan, Ju Liu, Yanlei Wang, Xingming Jie, Jingyu Qin, Hongyan He.  (2022)  Ionic liquids enable highly efficient Knoevenagel reaction by dual-responsive emulsion microreactor.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.138941]
7. Zhaoxian Tang, Yanjing Gao, Shengling Jiang, Jun Nie, Fang Sun.  (2022)  Cinnamoylformate derivatives photoinitiators with excellent photobleaching ability and cytocompatibility for visible LED photopolymerization.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2022.106969]
8. Yan Chen, Zhao Mo, Xingtong Zhu, Qingxiang Xu, Zhaoli Xue, Henan Li, Hui Xu, Long Zhao.  (2021)  Facilitated interfacial charge separation using triphenylamine-zinc porphyrin dyad-sensitized TiO2 nanoparticles for photocatalysis.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2021.161795]
9. Xiaoyan Pei, Jiang Liu, Weihao Rao, Xiantao Ma, Zhiyong Li.  (2021)  CO2-Switchable Reversible Phase Transfer of Carbon Dots.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.1c01287]
10. Long Zhao, Qingxiang Xu, Zhiwen Shao, Yan Chen, Zhaoli Xue, Henan Li, Jianming Zhang.  (2020)  Enhanced Oxygen Reduction Reaction Performance Using Intermolecular Forces Coupled with More Exposed Molecular Orbitals of Triphenylamine in Co-porphyrin Electrocatalysts.  ACS Applied Materials & Interfaces,      [PMID:32975398] [10.1021/acsami.0c11742]
11. Zhu Anlian, Li Qixing, Feng Wanlu, Fan Dongshuang, Li Lingjun.  (2020)  Biocompatible Ionic Liquid Promote One-Pot Synthesis of 2-Amino-4H-Chromenes Under Ambient Conditions.  CATALYSIS LETTERS,  151  (3): (720-733).  [PMID:] [10.1007/s10562-020-03332-7]
12. Lu Yan, Chang Zhaosen, Zhang Shizhen, Wang Shunli, Chen Qi, Feng Lijuan, Sui Zhuyin.  (2020)  Porous organic polymers containing zinc porphyrin and phosphonium bromide as bifunctional catalysts for conversion of carbon dioxide.  JOURNAL OF MATERIALS SCIENCE,  55  (26): (11856-11869).  [PMID:] [10.1007/s10853-020-04851-9]
13. Xiaoji Cao, Mei Fang, Danqi Dong, Beibei Ye, Jiahui Xu, Xuemin Ye, Weimin Mo.  (2020)  Dispersive liquid–liquid extraction based on magnetic Pickering emulsion followed by gas chromatography–tandem mass spectrometry for the simultaneous determination of aldehydes in environmental water samples.  JOURNAL OF SEPARATION SCIENCE,  43  (12): (2401-2408).  [PMID:32160648] [10.1002/jssc.201901150]
14. Lianqing Chen, Zhongda Wu, Yanting Du, Yufeng Huang, Shiwei Jin.  (2019)  Solvothermal synthesis of novel phenylpyrazole Schiff base fluorescent insecticides fused extended conjugate units for enhancing bioactivities, photophysical and electrochemical properties.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2019.06.093]
15. Geng Yang, Xia Meng, Shimin Fang, Hongdong Duan, Lizhen Wang, Zhenzheng Wang.  (2019)  A highly selective colorimetric fluorescent probe for detection of Hg2+ and its application on test strips.  RSC Advances,  (15): (8529-8536).  [PMID:35518693] [10.1039/C9RA00797K]
16. Wang Fanwei, Duan Hongdong, Xing Dianxiang, Yang Geng.  (2017)  Novel Turn-on Fluorescence Probes for Al3+ Based on Conjugated Pyrazole Schiff Base.  JOURNAL OF FLUORESCENCE,  27  (5): (1721-1727).  [PMID:28497408] [10.1007/s10895-017-2110-6]
17. Xiang-Lan Wang, Yuan-Xia Li, Shuai-Liang Yang, Chen-Xi Zhang, Qing-Lun Wang.  (2017)  Two copper complexes based on nitronyl nitroxide with different halides: structures and magnetic properties.  JOURNAL OF COORDINATION CHEMISTRY,      [PMID:] [10.1080/00958972.2016.1271417]
18. Yuanyuan Yue, Qiao Dong, Yajie Zhang, Xiaoge Li, Xuyang Yan, Yahui Sun, Jianming Liu.  (2015)  Synthesis of imidazole derivatives and the spectral characterization of the binding properties towards human serum albumin.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:26474241] [10.1016/j.saa.2015.09.023]
19. Benlin Hu, Fei Zhuge, Xiaojian Zhu, Shanshan Peng, Xinxin Chen, Liang Pan, Qing Yan, Run-Wei Li.  (2011)  Nonvolatile bistable resistive switching in a new polyimide bearing 9-phenyl-9H-carbazole pendant.  JOURNAL OF MATERIALS CHEMISTRY,  22  (2): (520-526).  [PMID:] [10.1039/C1JM13849A]
20. Tianyu Li, Shiyang Yi, Wenjie Sun, Yujie Liang, Hong Zheng, Zhongqi Guo, Yonghong Cheng, Lei Zhang.  (2024)  Constructing fluorinated triphenyl in carbonate copolymers toward flexible high energy-storable dielectric films with enhanced thermal resistance.  Nano Energy,      [PMID:] [10.1016/j.nanoen.2024.110105]
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