Description
2-Chloro-6-fluorobenzyl alcohol (CAS No. 56456-50-9) is a high-purity fluorinated and chlorinated benzyl alcohol derivative with the molecular formula C7H6ClFO. This compound, also known by its IUPAC name (2-chloro-6-fluorophenyl)methanol, is a versatile building block in organic synthesis and pharmaceutical research. The presence of both chloro and fluoro substituents on the aromatic ring enhances its reactivity, making it valuable for nucleophilic substitution reactions and as a precursor for more complex molecules. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied in sealed containers under inert atmosphere to guarantee stability. Ideal for medicinal chemistry, agrochemical development, and material science applications.
Properties
- CAS Number: 56456-50-9
- Complexity: 110
- IUPAC Name: (2-chloro-6-fluoro-phenyl)methanol
- InChI: InChI=1S/C7H6ClFO/c8-6-2-1-3-7(9)5(6)4-10/h1-3,10H,4H2
- InChI Key: ZZFCUESFXBCRSC-UHFFFAOYSA-N
- Exact Mass: 160.0091207
- Molecular Formula: C7H6ClFO
- Molecular Weight: 160.57
- SMILES: C1=CC(=C(C(=C1)Cl)CO)F
- Topological: 20.2
- Monoisotopic Mass: 160.0091207
- Synonyms: 2-Chloro-6-fluorobenzyl alcohol, 56456-50-9, (2-Chloro-6-fluorophenyl)methanol, 2-fluoro-6-chlorobenzyl alcohol, Benzenemethanol, 2-chloro-6-fluoro-, 2-Chloro-6-fluorobenzylic alcohol, 5K0SC480HM, EINECS 260-192-9, ZZFCUESFXBCRSC-UHFFFAOYSA-, DTXSID30205006, DTXCID90127497, 260-192-9, inchi=1/c7h6clfo/c8-6-2-1-3-7(9)5(6)4-10/h1-3,10h,4h2, MFCD00004608, 2-Chloro-6-fluorobenzylalcohol, UNII-5K0SC480HM, SCHEMBL697704, SCHEMBL3040407, 6-chloro-2-fluorobenzylic alcohol, CK2440, SBB056784, (2-Chloro-6-fluorophenyl)methanol #, AKOS000249061, (2-chloro-6-fluorophenyl)methan-1-ol, (6-chloro-2-fluorophenyl)methan-1-ol, CS-W016150, GF-0090, 2-Chloro-6-fluorobenzyl alcohol, 97%, AC-26175, SY018219, DB-020881, C1638, NS00054266, ST50406663, EN300-49125, Q27262475
Application
2-Chloro-6-fluorobenzyl alcohol serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and antibacterial agents. Its reactive benzylic alcohol group allows for facile conversion to aldehydes, halides, or esters, enabling diverse derivatization pathways. Researchers utilize this compound in Suzuki-Miyaura coupling reactions to construct biaryl scaffolds common in drug discovery. It is also employed in the preparation of liquid crystal materials due to its polarizable aromatic system.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (88.9%): 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 (100%)
- Eye Irrit. 2 (100%)
- STOT SE 3 (88.9%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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