Home Amines 76045-71-1
76045-71-1,MFCD06797571
Catalog No.:AA003ITQ
76045-71-1 | 3-Amino-5-hydroxybenzoic acid
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100mg
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250mg
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA003ITQ
Chemical Name:
3-Amino-5-hydroxybenzoic acid
CAS Number:
76045-71-1
Molecular Formula:
C7H7NO3
Molecular Weight:
153.1354
MDL Number:
MFCD06797571
IUPAC Name:
3-amino-5-hydroxybenzoic acid
InChI:
InChI=1S/C7H7NO3/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,9H,8H2,(H,10,11)
InChI Key:
QPEJHSFTZVMSJH-UHFFFAOYSA-N
SMILES:
Nc1cc(O)cc(c1)C(=O)O
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:
153.043g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
153.137g/mol
Monoisotopic Mass:
153.043g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
83.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  

Synonyms
 
3-AHBA 
3-amino-5-hydroxybenzoic acid 
PubChem17213 
AC1Q5TRR 
AC1L2RH3 
AC1Q51QR 
3-amino-5-hydoxybenzoic acid 
3-Amino-5-hydroxybenzoicAcid 
SCHEMBL571808 
CHEBI:29507 
CTK5E2411 
DTXSID20226947 
3-Amino-5-hydroxybenzoic acid 
Benzoic acid,3-amino-5-hydroxy- 
QPEJHSFTZVMSJH-UHFFFAOYSA-N 
ZINC968065 
KS-00000CB0 
ANW-61669 
FCH835445 
MFCD06797571 
AKOS005257914 
AB29674 
AC-2634 
76045-71-1 
QC-9268 
TRA0066062 
AJ-24571 
AN-13791 
AS-31231 
SC-20095 
SY002353 
AB0062037 
AX8084285 
DB-018515 
3-Ahba 
ST2417468 
TC-150414 
4CH-015464 
FT-0696241 
Z5106 
C12107 
M-8350 
MFCD06797571 (97+%) 
I14-17432 
3-amino-5-hydroxybenzoate 
AHBA 
C7H7NO3 
AR-1F1844 
CID127115 
Benzoic acid, 3-amino-5-hydroxy- (9CI) 
8012-02-0 
Benzoic acid, 3-amino-5-hydroxy- 
3-amino-5-hydroxy-benzoic acid 
AK-36312 
119690-81-2 
Literature

Title: Biosynthesis of 3,5-AHBA-derived natural products.

Journal: Natural product reports 20120201

Title: Broad substrate specificity of the amide synthase in S. hygroscopicus--new 20-membered macrolactones derived from geldanamycin.

Journal: Journal of the American Chemical Society 20120125

Title: Cloning and functional analysis of the naphthomycin biosynthetic gene cluster in Streptomyces sp. CS.

Journal: Molecular bioSystems 20110801

Title: Chaxamycins A-D, bioactive ansamycins from a hyper-arid desert Streptomyces sp.

Journal: Journal of natural products 20110624

Title: Mutational biosynthesis of ansamitocin antibiotics: a diversity-oriented approach to exploit biosynthetic flexibility.

Journal: Chembiochem : a European journal of chemical biology 20110307

Title: The biosynthesis of 3-amino-5-hydroxybenzoic acid (AHBA), the precursor of mC7N units in ansamycin and mitomycin antibiotics: a review.

Journal: The Journal of antibiotics 20110101

Title: Engineered polyketide biosynthesis and biocatalysis in Escherichia coli.

Journal: Applied microbiology and biotechnology 20101201

Title: New, highly active nonbenzoquinone geldanamycin derivatives by using mutasynthesis.

Journal: Chembiochem : a European journal of chemical biology 20090720

Title: Antitumor compounds from marine actinomycetes.

Journal: Marine drugs 20090601

Title: Synthesis of potential early-stage intermediates in the biosynthesis of FR900482 and mitomycin C.

Journal: Organic letters 20090219

Title: Biosynthesis of diazepinomicin/ECO-4601, a Micromonospora secondary metabolite with a novel ring system.

Journal: Journal of natural products 20080901

Title: Highly active ansamitocin derivatives: mutasynthesis using an AHBA-blocked mutant.

Journal: Chembiochem : a European journal of chemical biology 20080505

Title: Biosynthesis of rubradirin as an ansamycin antibiotic from Streptomyces achromogenes var. rubradiris NRRL3061.

Journal: Archives of microbiology 20080501

Title: Hydroxyquinone O-methylation in mitomycin biosynthesis.

Journal: Journal of the American Chemical Society 20070523

Title: Biosynthesis of tetrapetalones.

Journal: Organic & biomolecular chemistry 20070521

Title: An integrative expression vector for Actinosynnema pretiosum.

Journal: BMC biotechnology 20070101

Title: Determination of the cryptic stereochemistry of the first PKS chain-extension step in ansamitocin biosynthesis by Actinosynnema pretiosum.

Journal: Chembiochem : a European journal of chemical biology 20060801

Title: Production of ansamycin polyketide precursors in Escherichia coli.

Journal: The Journal of antibiotics 20060801

Title: Stereochemical assignment of intermediates in the rifamycin biosynthetic pathway by precursor-directed biosynthesis.

Journal: Journal of the American Chemical Society 20050817

Title: Transformation of the antibacterial agent sulfamethoxazole in reactions with chlorine: kinetics, mechanisms, and pathways.

Journal: Environmental science & technology 20041101

Title: Kanosamine biosynthesis: a likely source of the aminoshikimate pathway's nitrogen atom.

Journal: Journal of the American Chemical Society 20020911

Title: Characterization of the early stage aminoshikimate pathway in the formation of 3-amino-5-hydroxybenzoic acid: the RifN protein specifically converts kanosamine into kanosamine 6-phosphate.

Journal: Journal of the American Chemical Society 20020911

Title: The loading and initial elongation modules of rifamycin synthetase collaborate to produce mixed aryl ketide products.

Journal: Biochemistry 20020423

Title: Biosynthesis of 1-deoxy-1-imino-D-erythrose 4-phosphate: a defining metabolite in the aminoshikimate pathway.

Journal: Journal of the American Chemical Society 20020130

Title: The loading module of rifamycin synthetase is an adenylation-thiolation didomain with substrate tolerance for substituted benzoates.

Journal: Biochemistry 20010522

Title: Mutational analysis and reconstituted expression of the biosynthetic genes involved in the formation of 3-amino-5-hydroxybenzoic acid, the starter unit of rifamycin biosynthesis in amycolatopsis Mediterranei S699.

Journal: The Journal of biological chemistry 20010420

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