Cyclofenil diphenol

Application 8-Cyclopentyl-1,3-dipropylxanthine has been used as an adenosine receptor (A1AR) antagonist in macrophages and human umbilical vein endothelial cells (HUVECs). It has also been used as A1AR antagonist in MCF-7 breast cancer cell line to

Application 8-Cyclopentyl-1,3-dipropylxanthine has been used as an adenosine receptor (A1AR) antagonist in macrophages and human umbilical vein endothelial cells (HUVECs). It has also been used as A1AR antagonist in MCF-7 breast cancer cell line to

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034 . This CRM is traceable to primary material from an NMI, e.

Analysis Note Assay (GC, area%): &#8805 99.0 % (a/a) Water (K.

Cyclohexylacetylene (Ethynylcyclohexane) mediates NADPH-dependent loss of cytochrome P-450 on incubation with hepatic microsomes . Application Cyclohexylacetylene (Ethynylcyclohexane) was used in the preparation of

Cyclohexylacetylene (Ethynylcyclohexane) mediates NADPH-dependent loss of cytochrome P-450 on incubation with hepatic microsomes . Application Cyclohexylacetylene (Ethynylcyclohexane) was used in the preparation of

Cyclohexylallene

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 24 &#176C Melting range (upper value): &#8804 28 &#176C Identity (IR): passes test Due to its specific melting range the product may be solid, liquid, a

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 24 &#176C Melting range (upper value): &#8804 28 &#176C Identity (IR): passes test Due to its specific melting range the product may be solid, liquid, a

Application Diphenyl N -cyanocarbonimidate has been used in the preparation of: N -substituted 2-amino-4 H -3,1-benzoxazines cyanoguanidine derivatives oxadiazoles

Application Reactant for: Three-component cyclization Probing coordination ability via a palladium pincer complex Chelation-assisted hydroacylation of olefins with primary alcohols Reactant for synthesis of: Trinuclear ruthenium carbonyl