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248231

Sigma-Aldrich

2-Amino-4-methylbenzophenone

99%

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About This Item

Linear Formula:
H2NC6H3(CH3)C(O)C6H5
CAS Number:
4937-62-6
Molecular Weight:
211.26
EC Number:
225-577-8
MDL number:
MFCD00007816
UNSPSC Code:
12352100
PubChem Substance ID:
24854923
NACRES:
NA.22

Assay

99%

mp

65-66 °C (lit.)

SMILES string

Cc1ccc(c(N)c1)C(=O)c2ccccc2

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

InChI key

YINYAGBOKBLJHY-UHFFFAOYSA-N

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKAA2682V
MKBB0355
MKAA2682
13529CD
17913CO

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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)
Synthesis of substituted 2-pyridyl-4-phenylquinolines.
Mamo A, et al.
Molecules (Basel), 7(8), 618-627 (2002)

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