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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)-

Benzoic acid, 2-amino-5-hydroxy-, methyl ester

COC(=O)c1cc(O)ccc1N Request for Quotation
Chemical Name: Benzoic acid, 2-amino-5-hydroxy-, methyl ester
CAS Number: 1882-72-0
Product Number: AG002GRN(AGN-PC-0JWJFP)
Synonyms:
MDL No:
Molecular Formula: C8H9NO3
Molecular Weight: 167.1620

Identification/Properties

Properties
MP:
157 - 159 °C
BP:
357.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
167.164g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
167.058g/mol
Monoisotopic Mass:
167.058g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
172
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-amino-5-hydroxybenzoate, also known as methyl anthranilate, is a versatile compound widely used in chemical synthesis processes. This compound serves as a key building block in the production of various organic compounds due to its unique chemical properties.In chemical synthesis, Methyl 2-amino-5-hydroxybenzoate acts as a precursor for the synthesis of pharmaceuticals, fragrances, and dyes. Its aromatic structure and functional groups make it a valuable starting material for the creation of a wide range of compounds with diverse applications.One important application of Methyl 2-amino-5-hydroxybenzoate is in the synthesis of fragrances. Its pleasant odor profile and compatibility with other fragrance components make it a popular choice for creating perfumes, lotions, and other scented products. Additionally, this compound is utilized in the production of dyes, where its structure can be modified to impart specific colors and properties to the final product.Furthermore, Methyl 2-amino-5-hydroxybenzoate plays a crucial role in pharmaceutical synthesis. Its involvement in the creation of active pharmaceutical ingredients (APIs) showcases its importance in the development of medications for various therapeutic purposes.Overall, the high versatility and reactivity of Methyl 2-amino-5-hydroxybenzoate make it an indispensable compound in chemical synthesis, offering a wide range of applications in industries such as fragrance, dye, and pharmaceutical manufacturing.