Oxazol-2-yl-phenylmethanol
Oxazol-2-yl-phenylmethanol (CAS: 130552-00-0; Formula: C10H9NO2; Molar Mass: 175.18 g/mol) is a heterocyclic organic compound. It serves as a valuable building block in chemical synthesis, particularly for the creation of more complex molecules. Its oxazole ring and methanol substituent offer versatile reactivity for organic chemists engaged in research and development.

Pharmaceutical Intermediate Synthesis
Utilised as a key intermediate in the synthesis of novel pharmaceutical compounds, leveraging its heterocyclic structure for drug discovery and development.
Organic Synthesis Building Block
Serves as a versatile reagent in general organic synthesis, enabling the construction of complex molecular architectures in research laboratories.
Heterocyclic Chemistry Research
Employed in academic and industrial research focused on oxazole chemistry and the development of new heterocyclic scaffolds.
| Molecular weight | 175.18 |
|---|---|
| Empirical formula | C10H9NO2 |
| Assay | 97% |
| Melting point | 88-92 °C(lit.) |

Hazard statements
- H302Harmful if swallowed
- H319Causes serious eye irritation
Precautionary statements
- P305IF IN EYES
| Protective equipment | dust mask type N95 (US), Eyeshields, Gloves |
|---|---|
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | Xn |
| Risk statements (R) | 22-36 |
| Safety statements (S) | 26-36 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Oxazol-2-yl-phenylmethanol used for?
+
Oxazol-2-yl-phenylmethanol is primarily used as a building block in organic synthesis, particularly in the pharmaceutical and heterocyclic chemistry sectors for research and development.
What are the CAS number and chemical formula for Oxazol-2-yl-phenylmethanol?
+
The CAS number is 130552-00-0 and the chemical formula is C10H9NO2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Oxazol-2-yl-phenylmethanol with a minimum assay of 97%. This product is supplied for research and laboratory use and is not represented as USP, BP, EP, or any other pharmacopoeial grade.
What are the main hazards associated with Oxazol-2-yl-phenylmethanol?
+
Oxazol-2-yl-phenylmethanol is classified as harmful if swallowed (H302) and causes serious eye irritation (H319). Appropriate personal protective equipment, including a dust mask (N95), eyeshields, and gloves, should be used during handling.
How is Oxazol-2-yl-phenylmethanol packed and shipped?
+
Products are carefully packed according to international shipping regulations. Tech Serve Solutions exports globally, ensuring compliant and secure delivery of chemical reagents.
How can I request a quote or sample for Oxazol-2-yl-phenylmethanol?
+
To request a quote or sample, please contact our sales department via the website or provided contact details, specifying the product name and CAS number.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis