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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)-

tert-Butyl 4-amino-3-methylbenzoate

O=C(c1ccc(c(c1)C)N)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl 4-amino-3-methylbenzoate
CAS Number: 934481-43-3
Product Number: AG0063CY(AGN-PC-0WAMNI)
Synonyms:
MDL No: MFCD08703398
Molecular Formula: C12H17NO2
Molecular Weight: 207.2689

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
207.273g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
207.126g/mol
Monoisotopic Mass:
207.126g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
232
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl 4-amino-3-methylbenzoate is a versatile compound commonly utilized in chemical synthesis reactions. This compound is valued for its ability to act as a building block in the creation of various organic compounds. In particular, tert-Butyl 4-amino-3-methylbenzoate serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, tert-Butyl 4-amino-3-methylbenzoate can undergo different transformations to introduce specific functional groups or structural motifs into the desired final product. This compound can participate in reactions such as acylation, alkylation, and condensation to create more complex molecules with increased molecular diversity.Moreover, tert-Butyl 4-amino-3-methylbenzoate's unique structural properties make it a valuable reagent for building molecular libraries for drug discovery and development purposes. Its presence in the synthesis route can influence the pharmacological properties of the final compound, making it a crucial component in medicinal chemistry research.Overall, tert-Butyl 4-amino-3-methylbenzoate plays a significant role in chemical synthesis by enabling the efficient construction of various organic molecules with diverse applications in pharmaceutical, agricultural, and other industries.