Description

2-Chloro-6-fluorobenzaldehyde (CAS No. 387-45-1) is a high-purity aromatic aldehyde with the molecular formula C₇H₄ClFO. This compound is a valuable building block in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring both chloro and fluoro substituents on the benzaldehyde ring, enables selective functionalization for the development of complex molecules. Our product is rigorously tested to ensure >98% purity (GC), with stringent quality controls to meet the demands of research and industrial applications. Available in various packaging options, from grams to kilograms, to suit your laboratory or production needs.

Key Features:

• High purity (>98% by GC)
• Stable under recommended storage conditions
• Versatile intermediate for cross-coupling reactions
• Compatible with Grignard, Wittig, and reductive amination reactions

Properties

• CAS Number: 387-45-1
• Complexity: 129
• IUPAC Name: 2-chloro-6-fluoro-benzaldehyde
• InChI: InChI=1S/C7H4ClFO/c8-6-2-1-3-7(9)5(6)4-10/h1-4H
• InChI Key: OACPOWYLLGHGCR-UHFFFAOYSA-N
• Exact Mass: 157.9934706
• Molecular Formula: C7H4ClFO
• Molecular Weight: 158.56
• SMILES: C1=CC(=C(C(=C1)Cl)C=O)F
• Topological: 17.1
• Monoisotopic Mass: 157.9934706
• Synonyms: 2-Chloro-6-fluorobenzaldehyde, Benzaldehyde, 2-chloro-6-fluoro-, EINECS 206-860-5, UNII-51YJ9BW8W7, 2-fluoro-6-chlorobenzaldehyde, 51YJ9BW8W7, DTXSID4022028, DTXCID002028, 206-860-5, oacpowyllghgcr-uhfffaoysa-n, 387-45-1, MFCD00003306, 2-Fluoro-6-chlorobenzaldehyde;, 6-CHLORO-2-FLUOROBENZALDEHYDE, 2-chloro-6-fluoro-benzaldehyde, 2chloro-6-fluorobenzaldehyde, 6-Fluoro-2-chlorobenzaldehyde, SCHEMBL154430, SCHEMBL535572, 2-fluoro-6-chloro-benzaldehyde, SBB040205, STK801562, 2-Chloro-6-fluorobenzaldehyde, 95%, AKOS000118947, AC-2667, CS-W016193, FC16013, HY-W015477, PS-8805, BP-10748, SY002480, DB-023958, C1424, NS00041775, ST50208666, EN300-19135, Q27260932, F2190-0601, Z104472904

Application

2-Chloro-6-fluorobenzaldehyde serves as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with antimicrobial or anti-inflammatory properties. It is also utilized in agrochemical research for creating novel pesticides and herbicides due to its halogenated aromatic structure. Researchers value this compound for its reactivity in palladium-catalyzed cross-coupling reactions, enabling the construction of complex biaryl systems.

Safety and Hazards

GHS Hazard Statements

• H315 (96.1%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (96.1%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (92.2%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (96.1%)
• Eye Irrit. 2 (96.1%)
• STOT SE 3 (92.2%)

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.