248231
2-Amino-4-methylbenzophenone
99%
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About This Item
Linear Formula:
H2NC6H3(CH3)C(O)C6H5
CAS Number:
Molecular Weight:
211.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-577-8
MDL number:
Assay:
99%
assay
99%
InChI key
YINYAGBOKBLJHY-UHFFFAOYSA-N
InChI
1S/C14H13NO/c1-10-7-8-12(13(15)9-10)14(16)11-5-3-2-4-6-11/h2-9H,15H2,1H3
SMILES string
Cc1ccc(c(N)c1)C(=O)c2ccccc2
mp
65-66 °C (lit.)
Application
2-Amino-4-methylbenzophenone has been used as starting reagent in the synthesis of:
- 4-phenyl-7-methyl-2-(2′-pyridyl)quinoline and 4-phenyl-7-methyl-2-[2′-(6′-methyl)pyridyl]-quinoline
- N-tert-butyl-2-{3(R)-[3-(3-chlorophenyl)ureido]-8-methyl-2-oxo-5(R)-phenyl-1,3,4,5-tetrahydrobenz[b]azepin-1-yl}acetamide
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of substituted 2-pyridyl-4-phenylquinolines.
Mamo A, et al.
Molecules (Basel), 7(8), 618-627 (2002)
Efficient Synthesis of N-tert-Butyl-2-{3 (R)-[3-(3-chlorophenyl) ureido]-8-methyl-2-oxo-5 (R)-phenyl-1, 3, 4, 5-tetrahydrobenz [b] azepin-1-yl} acetamide and Related CCKB Antagonists.
Urban FJ, et al.
Organic Process Research & Development, 1(2), 131-136 (1997)
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