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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-(5,6-dichloropyridin-3-yl)carbamate

O=C(OC(C)(C)C)Nc1cnc(c(c1)Cl)Cl Request for Quotation
Chemical Name: tert-butyl N-(5,6-dichloropyridin-3-yl)carbamate
CAS Number: 275383-96-5
Product Number: AG002U0T(AGN-PC-03S08M)
Synonyms:
MDL No:
Molecular Formula: C10H12Cl2N2O2
Molecular Weight: 263.1205

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
263.118g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
262.028g/mol
Monoisotopic Mass:
262.028g/mol
Topological Polar Surface Area:
51.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
256
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


The tert-Butyl (5,6-dichloropyridin-3-yl)carbamate is a versatile compound widely used in chemical synthesis processes. Its unique properties make it an invaluable tool for organic chemists working in a variety of fields. In organic synthesis, this compound serves as a key building block for the creation of complex molecules and pharmaceutical compounds. Due to its stability and reactivity, tert-Butyl (5,6-dichloropyridin-3-yl)carbamate is particularly well-suited for reactions that require a selective and controlled approach. Its introduction into a reaction can facilitate the formation of new bonds and functional groups, leading to the production of desired products with high efficiency and purity. In medicinal chemistry, this compound plays a crucial role in the development of novel drug candidates with potential therapeutic applications. Researchers rely on its unique structure and reactivity to design and synthesize molecules with specific pharmacological properties. Overall, the application of tert-Butyl (5,6-dichloropyridin-3-yl)carbamate in chemical synthesis enables the rapid and precise construction of complex molecules, making it an indispensable tool for modern organic chemistry research.