Home Iodos 119-30-2
119-30-2,MFCD00002458
Catalog No.:AA003HC0
119-30-2 | 2-Hydroxy-5-iodobenzoic acid
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1g
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5g
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25g
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HC0
Chemical Name:
2-Hydroxy-5-iodobenzoic acid
CAS Number:
119-30-2
Molecular Formula:
C7H5IO3
Molecular Weight:
264.0173
MDL Number:
MFCD00002458
IUPAC Name:
2-hydroxy-5-iodobenzoic acid
InChI:
InChI=1S/C7H5IO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)
InChI Key:
SWDNKOFGNPGRPI-UHFFFAOYSA-N
SMILES:
Ic1ccc(c(c1)C(=O)O)O
EC Number:
204-313-5
NSC Number:
2789
Properties
Computed Properties
 
Complexity:
160  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
263.928g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
264.018g/mol
Monoisotopic Mass:
263.928g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
57.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  

Synonyms
 
5-iodosalicylic acid 
5-iodosalicylic acid sodium salt 
MFCD00002458 
BRN 2090443 
2-hydroxy-5-iodo-benzoic acid 
RARECHEM AL BE 0824 
SWDNKOFGNPGRPI-UHFFFAOYSA-N 
LABOTEST-BB LT00454718 
5-Jod-salicylsaure 
5-IodosalicylicAcid 
5-iodo-salicylicaci 
5-iodinsalicylic acid 
5-Iodosalicylic acid 
5-iodosalicyclic acid 
PubChem3889 
5-IODSALICYLSAEURE 
WLN: QVR BQ EI 
ACMC-1BNN4 
AC1L1QW5 
5-Iodosalycilic acid, Tech. 
SCHEMBL129664 
AC1Q72I8 
CHEMBL3278559 
2-Hydroxy-5-iodobenzoic acid 
CTK3J2536 
DTXSID10152281 
NSC2789 
ZINC156387 
BCP24359 
NSC-2789 
ANW-17308 
LABOTEST-BB LT03333603 
LABOTEST-BB LT03380782 
SBB057928 
119-30-2 
5-Iodosalicylic acid, technical grade 
AKOS000121006 
AS02197 
MCULE-9277488598 
NE10197 
KS-000011S7 
AC-23694 
AJ-13786 
AN-43298 
AT-13633 
Benzoic acid, 2-hydroxy-5-iodo- 
BP-11486 
Benzoic acid, 2-hydroxy-5-iodo- (9CI) 
AB0011184 
DB-014579 
LS-144342 
RT-000712 
TL8000513 
FT-0620519 
I0538 
ST45028976 
SALICYLIC ACID, 5-IODO- 
I01-5264 
W-108520 
F0001-0305 
InChI=1/C7H5IO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11 
C7H5IO3 
2-Hydroxy-5-iodobenzoicacid 
5-iodosalicylic acid sodium salt 
CID8388 
C7-H5-I-O3 
4-27-00-07537 (Beilstein Handbook Reference) 
5-IODO-2-HYDROXYBENZOIC ACID 
C017429 
NSC 2789 
EINECS 204-313-5 
Literature

Title: Iodination of salicylic acid improves its binding to transthyretin.

Journal: Biochimica et biophysica acta 20080301

Title: Analysis of the involvement of human N-acetyltransferase 1 in the genotoxic activation of bladder carcinogenic arylamines using a SOS/umu assay system.

Journal: Mutation research 20041004

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