Skip to Content
Merck
All Photos(1)

Documents

562440

Sigma-Aldrich

6-Aminobenzothiazole

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C7H6N2S
CAS Number:
Molecular Weight:
150.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

87-91 °C (lit.)

SMILES string

Nc1ccc2ncsc2c1

InChI

1S/C7H6N2S/c8-5-1-2-6-7(3-5)10-4-9-6/h1-4H,8H2

InChI key

FAYAYUOZWYJNBD-UHFFFAOYSA-N

General description

6-Aminobenzothiazole can be prepared from 6-nitrobenzothiazole via sonochemical reduction method.

Application

6-Aminobenzothiazole may be used in the synthesis of following:
  • 1-(6-amino-benzothiazolyl)-3-chloro-5-methoxytriazine
  • 6-[(4-N,N-dimethylaminophenyl)diazenyl]benzothiazole
  • 6-[(2-hydroxy-1-naphthyl)diazenyl]benzothiazole
  • 6-dimethylaminobenzothiazole

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

"2-Hydroxy-4, 6-diamino-[1, 3, 5] triazines: a novel class of VEGF-R2 (KDR) tyrosine kinase inhibitors"
Baindur N, et al.
Journal of Medicinal Chemistry, 48(6), 1717-1720 (2005)
"Preparation of novel push-pull benzothiazole derivatives with reverse polarity: compounds with potential non-linear optic application"
Hrobarik P, et al.
Synthesis, 2005(04), 600-604 (2005)
?The synthesis and structural study of two benzothiazolyl azo dyes: X-ray crystallographic and computational study of azo?hydrazone tautomerism?
Pavlovic G, et al.
Dyes and Pigments, 83(3), 354-362 (2009)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service