Home Aminos 3,4-Diaminobenzoic acid

3,4-Diaminobenzoic acid

CAS No.:
619-05-6
Catalog Number:
AG003IFG
Molecular Formula:
C7H8N2O2
Molecular Weight:
152.1506
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
~90%
In Stock USA
United States
$54
- +
500g
~90%
In Stock USA
United States
$123
- +
Product Description
Catalog Number:
AG003IFG
Chemical Name:
3,4-Diaminobenzoic acid
CAS Number:
619-05-6
Molecular Formula:
C7H8N2O2
Molecular Weight:
152.1506
MDL Number:
MFCD00007726
IUPAC Name:
3,4-diaminobenzoic acid
InChI:
InChI=1S/C7H8N2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,8-9H2,(H,10,11)
InChI Key:
HEMGYNNCNNODNX-UHFFFAOYSA-N
SMILES:
OC(=O)c1ccc(c(c1)N)N
EC Number:
210-577-2
UNII:
2H2G880K12
Properties
Complexity:
161  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
152.059g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
152.153g/mol
Monoisotopic Mass:
152.059g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
89.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  
Literature
Title Journal
A reversible protection strategy to improve Fmoc-SPPS of peptide thioesters by the N-Acylurea approach. Chembiochem : a European journal of chemical biology 20111104
The retention behaviour of polar compounds on zirconia based stationary phases under hydrophilic interaction liquid chromatography conditions. Journal of chromatography. A 20110928
Soluble monometallic salen complexes derived from O-functionalised diamines as metalloligands for the synthesis of heterobimetallic complexes. Dalton transactions (Cambridge, England : 2003) 20100507
Quantum dots improve peptide detection in MALDI MS in a size dependent manner. Journal of nanobiotechnology 20090101
Vibrational spectra and quantum chemical calculations of 3,4-diaminobenzoic acid. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080701
(99m)Tc complexes with activated ester functions; ligands comprising a 3,4-diamino-benzoate backbone. Nuclear medicine and biology 20060401
Interaction of mushroom tyrosinase with aromatic amines, o-diamines and o-aminophenols. Biochimica et biophysica acta 20040804
On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines. Organic & biomolecular chemistry 20031207
Reducing the alkali cation adductions of oligonucleotides using sol-gel-assisted laser desorption/ionization mass spectrometry. Analytical chemistry 20030815
Properties