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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 N-(5-formylpyrazin-2-yl)carbamate

O=Cc1ncc(nc1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-(5-formylpyrazin-2-yl)carbamate
CAS Number: 959617-71-1
Product Number: AG00IJOO(AGN-PC-0712VP)
Synonyms:
MDL No:
Molecular Formula: C10H13N3O3
Molecular Weight: 223.22852

Identification/Properties

Computed Properties
Molecular Weight:
223.232g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
223.096g/mol
Monoisotopic Mass:
223.096g/mol
Topological Polar Surface Area:
81.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
263
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


tert-Butyl (5-formylpyrazin-2-yl)carbamate is a versatile compound that finds wide application in chemical synthesis. With its unique molecular structure, this compound serves as a valuable building block in the preparation of various complex organic molecules. In synthetic chemistry, it is often utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and stability make it a preferred choice for the modification of functional groups in organic molecules. Additionally, tert-Butyl (5-formylpyrazin-2-yl)carbamate plays a crucial role in the development of novel chemical reactions and methodologies, contributing to the progress of organic synthesis. Its versatility and utility make it an indispensable component in the toolkit of synthetic chemists seeking to access diverse and challenging molecular structures.