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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)-

Acetamide, N-(2-amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-

CC(=O)NC1CCc2c(C1)sc(n2)N Request for Quotation
Chemical Name: Acetamide, N-(2-amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-
CAS Number: 104617-51-8
Product Number: AG007XQ5(AGN-PC-00NFDN)
Synonyms:
MDL No:
Molecular Formula: C9H13N3OS
Molecular Weight: 211.2840

Identification/Properties

Computed Properties
Molecular Weight:
211.283g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
211.078g/mol
Monoisotopic Mass:
211.078g/mol
Topological Polar Surface Area:
96.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
236
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Product Description:N-(2-Amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)acetamide is a versatile compound widely utilized in chemical synthesis for its unique properties. In the realm of organic chemistry, this compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features make it an essential precursor in the synthesis of complex molecules with diverse biological activities.This compound plays a crucial role in the development of novel drugs and therapeutic agents due to its ability to participate in key synthetic reactions. The presence of the amino and acetamide functional groups offers opportunities for selective functionalization, allowing chemists to tailor the compound for specific applications. By incorporating N-(2-Amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)acetamide into synthetic pathways, researchers can access a wide range of compounds with potential pharmaceutical benefits.Furthermore, this compound's unique molecular structure enables its use in the preparation of advanced materials and fine chemicals. Its aromatic thiazole ring provides opportunities for diversification through various chemical transformations, leading to the creation of novel molecules with tailored properties. Chemists leverage the reactivity of N-(2-Amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)acetamide to access structurally diverse compounds that find applications in fields ranging from materials science to medicinal chemistry.In summary, N-(2-Amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)acetamide plays a vital role in chemical synthesis by serving as a versatile intermediate for the construction of complex molecules with practical implications in pharmaceuticals, agrochemicals, and materials science. Its significance lies in its strategic position as a key building block for the creation of diverse compounds, highlighting its importance in advancing the frontiers of modern chemistry.