General description
3′-Aminoacetophenone acts as bifunctional coupling reagent during the synthesis of pyrimidines.
Application
3′-Aminoacetophenone (3-Acetylaniline) was used as reagent during the asymmetric total synthesis of pactamycin. It was used as starting reagent during the synthesis of curcumin mimics with substituted sulfonyl group.
Molecular Weight: 135.16. Empirical Formula: C8H9NO. linearFormula: H2NC6H4COCH3. Quality Level: 100. Assay: 97%. bp: 289-290 . °C (lit.). mp: 94-98 . °C (lit.). SMILES string: CC(: O)c1cccc(N)c1. InChI: 1S/C8H9NO/c1-6(10)7-3-2-4-8(9)5-7/h2-5H,9H2,1H3. InChI key: CKQHAYFOPRIUOM-UHFFFAOYSA-N. Pictograms: GHS07. Signal Word: Warning. Hazard Statements: H302. Precautionary Statements: P264 - P270 - P301 + P312 - P501. Hazard Classifications: Acute Tox. 4 Oral. Storage Class Code: 11 - Combustible Solids. WGK: WGK 2. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves.- UPC:
- 51142501
- Condition:
- New
- HazmatClass:
- No
- MPN:
- 139351-25G
- CAS:
- 99-03-6
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