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13036-02-7

13036-02-7 | 1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl ester

CAS No: 13036-02-7 Catalog No: AG000UB7 MDL No:MFCD00134367

Product Description

Catalog Number:
AG000UB7
Chemical Name:
1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl ester
CAS Number:
13036-02-7
Molecular Formula:
C10H10O5
Molecular Weight:
210.1834
MDL Number:
MFCD00134367
IUPAC Name:
dimethyl 5-hydroxybenzene-1,3-dicarboxylate
InChI:
InChI=1S/C10H10O5/c1-14-9(12)6-3-7(10(13)15-2)5-8(11)4-6/h3-5,11H,1-2H3
InChI Key:
DOSDTCPDBPRFHQ-UHFFFAOYSA-N
SMILES:
COC(=O)c1cc(O)cc(c1)C(=O)OC
EC Number:
235-899-0

Properties

Complexity:
226  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
210.053g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
210.185g/mol
Monoisotopic Mass:
210.053g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
72.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  

Literature

Title Journal
Solid-phase synthesis and acidolytic degradation of sterically congested oligoether dendrons. Organic & biomolecular chemistry 20120628
Tetra-methyl 5,5'-[4,5-dicyano-1,2-phenyl-enebis(-oxy)]diisophthalate chloro-form monosolvate. Acta crystallographica. Section E, Structure reports online 20110701
Enhanced Transport Capabilities via Nanotechnologies: Impacting Bioefficacy, Controlled Release Strategies, and Novel Chaperones. Journal of drug delivery 20110101
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Enzymatic synthesis of multi-component copolymers and their structural characterization. Molecular diversity 20030101

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