Controlled substance analgesic thiophenes

2-(2-Bromoacetyl)thiophene

2-(2-Bromoacetyl)thiophene

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Adsorption of 2-thiopheneacetic acid on XAD-4, NDA-100 and ND-90 resin has been investigated. A new polymeric complex of Cu(II) and 2-thiopheneacetic acid has been synthesized and characterized by IR and Raman spectroscopy .

Application 2-Thiopheneacetyl chloride was used in the synthesis of: ( S )-ethyl-1-(2-thiopheneacetyl)-3-piperidinecarboxylate, nipecotate-containing immunopotentiator 5-fluorouracil-cephalosporin prodrug series of new N , N

Application 2-Thiophenecarbonitrile (2-Cyanothiophene) was used in the preparation of thiaplatinacycles . It was also used in the synthesis of 2,2&#8242-thienylpyrroles .

Application 2-Thiophenecarbonitrile (2-Cyanothiophene) was used in the preparation of thiaplatinacycles . It was also used in the synthesis of 2,2&#8242-thienylpyrroles .

The postfunctionalization reaction of 2-thiophenecarbonyl chloride with single walled carbon nanotubes (SWCNTs) was studied . Application 2-Thiophenecarbonyl chloride was used in the synthesis of building blocks derived from ornithine by undergoing

The postfunctionalization reaction of 2-thiophenecarbonyl chloride with single walled carbon nanotubes (SWCNTs) was studied . Application 2-Thiophenecarbonyl chloride was used in the synthesis of building blocks derived from ornithine by undergoing

2-Thiopheneethylamine (2-(thiophen-2-yl)ethanamine) is an aromatic amine. It undergoes microwave induced condensation with iminodiacetic acid to form the corresponding piperazine-2,6-dione derivatives.