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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)-

5-Benzothiazolamine, 2-methyl-

Nc1ccc2c(c1)nc(s2)C Request for Quotation
Chemical Name: 5-Benzothiazolamine, 2-methyl-
CAS Number: 13382-43-9
Product Number: AG003HOP(AGN-PC-0JKOY0)
Synonyms:
MDL No:
Molecular Formula: C8H8N2S
Molecular Weight: 164.2275

Identification/Properties

Properties
MP:
215℃
BP:
325°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
164.226g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
164.041g/mol
Monoisotopic Mass:
164.041g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methylbenzo[d]thiazol-5-amine, also known as $name$, is a versatile compound commonly used in chemical synthesis processes. This compound plays a crucial role in various reactions and methodologies in the field of organic chemistry. One of the key applications of 2-Methylbenzo[d]thiazol-5-amine is its utility as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure allows for the modification and functionalization of the amine group, enabling the creation of diverse chemical compounds with a wide range of potential biological activities. Additionally, 2-Methylbenzo[d]thiazol-5-amine is often employed as a ligand in coordination chemistry, contributing to the development of novel metal complexes with enhanced catalytic properties. In summary, the versatility and reactivity of 2-Methylbenzo[d]thiazol-5-amine make it a valuable tool in the realm of chemical synthesis with broad applications across various industries.