6635-39-8

Basic information

• Product Name: Benzothiazole-2-yl azide
• Synonyms: 2-Azidobenzothiazole;Benzothiazole-2-yl azide
• CAS NO: 6635-39-8
• Molecular Formula: C₇H₄N₄S
• Molecular Weight: 0
• Mol File: 6635-39-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzothiazole-2-yl azide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole-2-yl azide(6635-39-8)
• EPA Substance Registry System: Benzothiazole-2-yl azide(6635-39-8)

Safety Data

• Hazardous Substances Data: 6635-39-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H5N4S/c8-11-10-7-9-5-3-1-2-4-6(5)12-7/h1-4,8H/q+1

Upstream product

• 615-20-3 2-chlorobenzo[d][1,3]thiazole 
• 941-55-9 4-toluenesulfonyl azide 
• 39582-59-7 benzothiazol-2-yl-lithium 
• 136-95-8 2-amino-benzthiazole 
• 1123-99-5 2-iodobenzothiazole 

Downstream Products

• 1400420-50-9 2-(4-(cyclohex-1-en-1-yl)-1H-1,2,3-triazol-1-yl)benzo[d]thiazole 
• 19747-95-6 2-[3-(triphenyl-λ⁵-phosphanylidene)-triaz-1-enyl]-benzothiazole 

Relevant articles and documents

Click chemistry inspired synthesis and bioevaluation of novel triazolyl derivatives of osthol as potent cytotoxic agents

A new series of diverse triazoles linked through the hydroxyl group of lactone ring opened osthol (1) were synthesized using click chemistry approach. All the derivatives were subjected to 3-(4,5-Dimethylthiazol-yl)-diphenyl tetrazoliumbromide (MTT) cytot

Development of benzothiazole 'click-on' fluorogenic dyes

'Click-on' fluorogenic reaction: a non-fluorescent benzothiazole with an electron-deficient alkyne group at 2-position reacts with azide containing molecules could form fluorescent adducts.

An easy access to aryl azides from aryl amines under neutral conditions

A variety of substituted aryl amines were transformed into aryl azides using t-BuONO and moist NaN3 in t-BuOH in good to excellent yields. Smooth transformation was observed with anilines, having electron withdrawing and donating groups. Both acid- and base-sensitive groups survived the reaction conditions. Georg Thieme Verlag Stuttgart.