37859-39-5

Basic information

• Product Name: 1,3-benzothiazol-2-ylmethyl phenyl ether
• Synonyms: 1,3-benzothiazol-2-ylmethyl phenyl ether
• CAS NO: 37859-39-5
• Molecular Formula: C₁₄H₁₁NOS
• Molecular Weight: 241.30824
• Mol File: 37859-39-5.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-benzothiazol-2-ylmethyl phenyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-benzothiazol-2-ylmethyl phenyl ether(37859-39-5)
• EPA Substance Registry System: 1,3-benzothiazol-2-ylmethyl phenyl ether(37859-39-5)

Safety Data

• Hazardous Substances Data: 37859-39-5(Hazardous Substances Data)

Upstream product

• 137-07-5 2-amino-benzenethiol 
• 122-59-8 2-phenoxyacetic acid 
• 701-99-5 Phenoxyacetyl chloride 
• 164408-46-2 2-methylthio-N-triphenylphosphoranylideneaniline 
• 35370-80-0 2-phenoxyethanethioamide 
• 37859-43-1 2-chloromethylbenzothiazole 
• 108-95-2 phenol 

Downstream Products

• 37859-45-3 3-methyl-2-phenoxymethyl-benzothiazolium; toluene-4-sulfonate 

Relevant articles and documents

IR, Raman and SERS spectra of 2-phenoxymethylbenzothiazole

The FT-IR and FT-Raman spectra of 2-phenoxymethylbenzothiazole were recorded and analyzed. The surface enhanced Raman scattering (SERS) spectrum was recorded in a silver colloid. The vibrational wavenumbers of the compound have been computed using the Har

An efficient acid- and metal-free one-pot synthesis of benzothiazoles from carboxylic acids

Carboxylic acids are converted to benzothiazoles in a one-pot reaction with thionyl chloride followed by treatment with 2-aminothiophenol under acid- and catalyst-free conditions. Georg Thieme Verlag Stuttgart.

Synthesis and structure-activity relationships of new antimicrobial active multisubstituted benzazole derivatives

A series of multisubstituted benzoxazoles, benzimidazoles, and benzothiazoles (5-7) as non-nucleoside fused isosteric heterocyclic compounds was synthesized and tested for their antibacterial activities against various Gram-positive and Gram-negative bacteria and antifungal activity against the fungus Candida albicans. Microbiological results indicated that the synthesized compounds possessed a broad spectrum of activity against the tested microorganisms at MIC values between 100 and 3.12 μg/ml. Structure-activity relationships (SAR) studies revealed that benzothiazole ring system enhanced the antimicrobial activity against Staphylococcus aureus. In these sets of non-nucleoside fused heterocyclic compounds electron withdrawing groups at position 5 of the benzazoles increased the activity against C. albicans.