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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)-

1H-Imidazole-1-carboxylic acid, 2-amino-, 1,1-dimethylethyl ester

O=C(n1ccnc1N)OC(C)(C)C Request for Quotation
Chemical Name: 1H-Imidazole-1-carboxylic acid, 2-amino-, 1,1-dimethylethyl ester
CAS Number: 929568-19-4
Product Number: AG003GC3(AGN-PC-0BTYUN)
Synonyms:
MDL No: MFCD20702858
Molecular Formula: C8H13N3O2
Molecular Weight: 183.2077

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
183.211g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
183.101g/mol
Monoisotopic Mass:
183.101g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
200
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-1-Boc-imidazole is a versatile chemical compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This compound acts as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. In particular, 2-Amino-1-Boc-imidazole is often employed as a building block in the synthesis of complex molecules, serving as a crucial starting point for the creation of diverse organic compounds. Its amino and imidazole functional groups allow for multiple synthetic pathways, enabling chemists to introduce specific substituents and structural motifs into target molecules.Furthermore, the Boc (tert-butoxycarbonyl) protective group present in 2-Amino-1-Boc-imidazole provides enhanced stability and control during chemical reactions, facilitating selective transformations and improving overall synthetic efficiency. This protective group can be easily removed under mild conditions, making it an ideal choice for strategically designing synthetic routes in modern organic chemistry.Overall, the application of 2-Amino-1-Boc-imidazole in chemical synthesis showcases its significance as a valuable building block for the construction of intricate molecular architectures with diverse functionalities. Its versatile nature and reactivity make it an indispensable tool for researchers and chemists in the development of novel compounds for various applications.