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2-Amino-6-bromobenzothiazole

ALDRICH/538507 - 97%

CAS Number: 15864-32-1
Empirical Formula (Hill Notation): C7H5BrN2S
Molecular Weight: 229.10
MDL Number: MFCD00152229
Linear Formula: C7H5BrN2S
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-538507-1G 1 g
 $32.70
1/EA		 Add To Favorites
45-538507-5G 5 g
 $55.70
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes, it may have been created or edited with AI. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 538507-5G

 

assay 97%
form solid
functional group bromo
InChI 1S/C7H5BrN2S/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H,(H2,9,10)
InChI key VZEBSJIOUMDNLY-UHFFFAOYSA-N
mp 213-217 °C (lit.)
Quality Level 100 
SMILES string Nc1nc2ccc(Br)cc2s1
Application: 2-Amino-6-bromobenzothiazole may be used in the synthesis of the following
• 2-amino-6-arylbenzothiazole compounds:
• 6-p-tolylbenzo[d]thiazole-2-amine
• 6-(4chlorophenyl)benzo[d]thiazole-2-amine
• 6-(4-methoxyphenyl)benzo[d]thiazole-2-amine
• 6-(3,5-bis(triflouromethyl)phenyl)benzo[d]thiazole-2-amine
• 6-phenylbenzo[d]thiazole-2-amine
It may be employed as a ligand (L) in the synthesis of organometallic derivatives of Rh(I) [Rh(CO)2(L)(Cl)].
General description: Reaction of 4-bromoaniline with acetic acid and potassium thiocynate in solution of bromine in acetic acid yields 2-amino-6-bromobenzothiazole. 2-Amino-6-bromobenzothiazole can also be synthesized from 2-aminobenzothiazole via monobromination with silica-supported quinolinium tribromide.
Packaging: 1, 5, 25 g in glass bottle
Purity 97%
mp 213-217 °C (lit.)
UNSPSC 12352100

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