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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,4-Benzodioxin-6-carboxylic acid, 7-amino-2,3-dihydro-

OC(=O)c1cc2OCCOc2cc1N Request for Quotation
Chemical Name: 1,4-Benzodioxin-6-carboxylic acid, 7-amino-2,3-dihydro-
CAS Number: 99358-09-5
Product Number: AG0065YZ(AGN-PC-0KPTW1)
Synonyms:
MDL No: MFCD06010010
Molecular Formula: C9H9NO4
Molecular Weight: 195.1721

Identification/Properties

Computed Properties
Molecular Weight:
195.174g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
195.053g/mol
Monoisotopic Mass:
195.053g/mol
Topological Polar Surface Area:
81.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
233
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Amino-2,3-dihydro-1,4-benzodioxin-6-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Due to its unique structure and properties, this compound plays a crucial role in various synthetic processes in the field of organic chemistry.One key application of 7-Amino-2,3-dihydro-1,4-benzodioxin-6-carboxylic acid is as a building block for the synthesis of heterocyclic compounds. Its amino group and carboxylic acid functionality make it an ideal starting material for the formation of complex structures with diverse reactivity. By undergoing selective functional group transformations, this compound can serve as a precursor for the synthesis of biologically active molecules, pharmaceuticals, and agrochemicals.Furthermore, the presence of the benzodioxin ring system in 7-Amino-2,3-dihydro-1,4-benzodioxin-6-carboxylic acid imparts specific properties that are beneficial for designing molecules with desired pharmacological or physicochemical attributes. This compound can participate in key bond-forming reactions such as amide bond formation, esterification, and cyclization, enabling the creation of novel chemical entities with potential applications in drug discovery and materials science.Overall, 7-Amino-2,3-dihydro-1,4-benzodioxin-6-carboxylic acid is a valuable intermediate in organic synthesis, facilitating the construction of diverse molecular architectures with tailored functionality and properties. Its versatility and reactivity make it a valuable tool for chemists seeking to design and prepare complex molecules for various industrial and research purposes.