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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-bromothiazol-5-yl)carbamate

O=C(Nc1cnc(s1)Br)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl (2-bromothiazol-5-yl)carbamate
CAS Number: 1094070-77-5
Product Number: AG0037YO(AGN-PC-080TYJ)
Synonyms:
MDL No:
Molecular Formula: C8H11BrN2O2S
Molecular Weight: 279.1541

Identification/Properties

Computed Properties
Molecular Weight:
279.152g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
277.972g/mol
Monoisotopic Mass:
277.972g/mol
Topological Polar Surface Area:
79.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
220
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-H332-H335
Precautionary Statements:
P261-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 (2-bromothiazol-5-yl)carbamate is a versatile compound widely utilized in chemical synthesis processes. As a key reactant in organic chemistry, this compound serves as a valuable building block for the creation of various complex molecules. Its unique structure and reactivity make it an important component in the synthesis of pharmaceuticals, agrochemicals, and materials science. By incorporating tert-Butyl (2-bromothiazol-5-yl)carbamate into reactions, chemists can access a diverse range of functional groups and stereoisomers, allowing for the efficient production of intricate molecular structures. Its utility in multiple synthetic pathways underscores its significance in modern chemical research and development.