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Home Other Building Blocks 2-Amino-5-methylbenzoic acid

2-Amino-5-methylbenzoic acid

CAS No.:
2941-78-8
Catalog Number:
AG003GHB
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$4
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$50
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG003GHB
Chemical Name:
2-Amino-5-methylbenzoic acid
CAS Number:
2941-78-8
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
MDL Number:
MFCD00007909
IUPAC Name:
2-amino-5-methylbenzoic acid
InChI:
InChI=1S/C8H9NO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,9H2,1H3,(H,10,11)
InChI Key:
NBUUUJWWOARGNW-UHFFFAOYSA-N
SMILES:
Cc1ccc(c(c1)C(=O)O)N
EC Number:
220-932-3
UNII:
418XAJ22V2
Properties
Complexity:
158  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
151.063g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
151.165g/mol
Monoisotopic Mass:
151.063g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
63.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.8  
Literature
Title Journal
3-Benzyl-6-methyl-2-sulfanylidene-2,3-di-hydroquinazolin-4(1H)-one. Acta crystallographica. Section E, Structure reports online 20120301
6-Methyl-3-phenyl-2-sulfanyl-idene-1,2,3,4-tetra-hydro-quinazolin-4-one. Acta crystallographica. Section E, Structure reports online 20120301
Localized auxin biosynthesis and postembryonic root development in Arabidopsis. Plant signaling & behavior 20090801
Synthesis and cytotoxicity screening of piperazine-1-carbodithioate derivatives of 2-substituted quinazolin-4(3H)-ones. Archiv der Pharmazie 20090301
Synthesis of substituted benzylamino- and heterocyclylmethylamino carbodithioate derivatives of 4-(3H)-quinazolinone and their cytotoxic activity. Archiv der Pharmazie 20060501
Toward a new genetic system with expanded dimensions: size-expanded analogues of deoxyadenosine and thymidine. Journal of the American Chemical Society 20040204
Properties