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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 2-amino-2-(3-bromophenyl)acetate

O=C(OC(C)(C)C)NCc1cccc(c1)Br Request for Quotation
Chemical Name: tert-butyl 2-amino-2-(3-bromophenyl)acetate
CAS Number: 171663-13-1
Product Number: AG003D2G(AGN-PC-0JEK26)
Synonyms:
MDL No: MFCD08703139
Molecular Formula: C12H16BrNO2
Molecular Weight: 286.1649

Identification/Properties

Properties
MP:
59-60°C
BP:
374.3±25.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
286.169g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
285.036g/mol
Monoisotopic Mass:
285.036g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 3-bromobenzylcarbamate is a versatile compound commonly used in chemical synthesis as a key building block for constructing various organic molecules. Its unique structure allows for selective functionalization at different positions, making it a valuable tool in synthetic chemistry.One of the main applications of tert-Butyl 3-bromobenzylcarbamate is in the synthesis of pharmaceutical intermediates and bioactive compounds. Its presence in a molecule can serve as a protecting group for sensitive functional groups, enabling specific reactions to take place at desired sites while preventing unwanted side reactions.Additionally, tert-Butyl 3-bromobenzylcarbamate can be utilized in cross-coupling reactions to introduce new functional groups or form complex carbon-carbon bonds. Its stability and reactivity make it a preferred reagent for creating intricate molecular structures in drug discovery and materials science.In essence, tert-Butyl 3-bromobenzylcarbamate is an indispensable tool for chemists seeking to design and synthesize novel compounds with tailored properties and functionalities for a wide range of applications.