24891-35-8,MFCD03147263
Catalog No.:AA002PP3

24891-35-8 | N-(3-Hydroxyphenyl)formamide

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  • Technical Information
  • Properties
  • Literature
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  • Download SDS
Technical Information
Catalog Number:
AA002PP3
Chemical Name:
N-(3-Hydroxyphenyl)formamide
CAS Number:
24891-35-8
Molecular Formula:
C7H7NO2
Molecular Weight:
137.1360
MDL Number:
MFCD03147263
SMILES:
O=CNc1cccc(c1)O
Properties
Computed Properties
 
Complexity:
116  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.9  

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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Tags:24891-35-8 Molecular Formula|24891-35-8 MDL|24891-35-8 SMILES|24891-35-8 N-(3-Hydroxyphenyl)formamide
Catalog No.: AA002PP3
24891-35-8,MFCD03147263
24891-35-8 | N-(3-Hydroxyphenyl)formamide
This product is typically in stock,please click "Inquire" below or contact us at [email protected]for pricing and availability information.
Inquire
Technical Information
Catalog Number: AA002PP3
Chemical Name: N-(3-Hydroxyphenyl)formamide
CAS Number: 24891-35-8
Molecular Formula: C7H7NO2
Molecular Weight: 137.1360
MDL Number: MFCD03147263
SMILES: O=CNc1cccc(c1)O
Properties
Complexity: 116  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.9  
Literature fold

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters20101101

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