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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-[4-(difluoromethyl)-1,3-thiazol-2-yl]carbamate

FC(c1csc(n1)NC(=O)OC(C)(C)C)F Request for Quotation
Chemical Name: tert-butyl N-[4-(difluoromethyl)-1,3-thiazol-2-yl]carbamate
CAS Number: 947179-19-3
Product Number: AG006T19(AGN-PC-07ASUP)
Synonyms:
MDL No:
Molecular Formula: C9H12F2N2O2S
Molecular Weight: 250.2656

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
250.264g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
250.059g/mol
Monoisotopic Mass:
250.059g/mol
Topological Polar Surface Area:
79.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
258
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 (4-(difluoromethyl)thiazol-2-yl)carbamate serves as a versatile building block in chemical synthesis, particularly valued for its ability to introduce the unique difluoromethylthiazole moiety into organic molecules. This compound is a key component in the construction of diverse chemical structures with potential applications in pharmaceuticals, agrochemicals, and materials science. Through strategic manipulation of its functional groups, researchers can access a wide array of derivatives and analogs, facilitating the discovery and development of novel compounds with tailored properties and enhanced biological activities. By incorporating tert-butyl (4-(difluoromethyl)thiazol-2-yl)carbamate into synthetic pathways, chemists can access a rich chemical space for exploring structure-activity relationships and molecular design, ultimately advancing the frontiers of organic chemistry and drug discovery.