mr-vis+ visual melting point range apparatus (Labindia Analytical Instrument)
90
Structured Review
Labindia Analytical Instrument
mr-vis+ visual melting point range apparatus
Mr Vis+ Visual Melting Point Range Apparatus, supplied by Labindia Analytical Instrument, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mr-vis++visual+melting+point+range+apparatus/visual+melting+range+apparatus/pmc09278343__SC___013___D2SC00046F___s001-20-5-12
Average 90 stars, based on 1 article reviews
Mr Vis+ Visual Melting Point Range Apparatus, supplied by Labindia Analytical Instrument, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mr-vis++visual+melting+point+range+apparatus/visual+melting+range+apparatus/pmc09278343__SC___013___D2SC00046F___s001-20-5-12
Average 90 stars, based on 1 article reviews
mr-vis+ visual melting point range apparatus - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: An umpolung strategy for intermolecular [2 + 2 + 1] cycloaddition of aryl aldehydes and nitriles: a facile access to 2,4,5-trisubstituted oxazoles Article Snippet: Melting points were determined on Article Title: Highly diastereoselective synthesis of tertiary alcohols via intramolecular Baylis-Hillman reaction using less reactive acrylamides as activated alkenes and ketones as electrophiles Article Snippet: Accepted Manuscript Highly diastereoselective synthesis of tertiary alcohols via intramolecular BaylisHillman reaction using less reactive acrylamides as activated alkenes and ketones as electrophiles Deevi Basavaiah, Guddeti Chandrashekar Reddy, Balthu Lingaiah, Ram Tilak Naganaboina PII: S0040-4020(16)31366-7 DOI: 10.1016/j.tet.2016.12.069 Reference: TET 28361 To appear in: Tetrahedron Received Date: 16 August 2016 Revised Date: 21 December 2016 Accepted Date: 26 December 2016 Please cite this article as: Basavaiah D, Reddy GC, Lingaiah B, Naganaboina RT, Highly diastereoselective synthesis of tertiary alcohols via intramolecular Baylis-Hillman reaction using less reactive acrylamides as activated alkenes and ketones as electrophiles, Tetrahedron (2017), doi: 10.1016/j.tet.2016.12.069.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript. Article Title: Synthesis and anion binding properties of the smallest meso-expanded calix[4]pyrrole Article Snippet: Melting points were determined by slides with coverslips on Article Title: Bis(pyrrole-benzimidazole) conjugates as novel colorimetric sensor for anions Article Snippet: Melting points were determined with Article Title: Synthesis and antimicrobial activity of 2‐(4‐(benzo[d]thiazol‐5‐ylsulfonyl)piperazine‐1‐yl)‐N‐substituted acetamide derivatives Article Snippet: A new series of 2-(4-(benzo[d]thiazol-5-ylsulfonyl) piperazin-1-yl)-N-substituted acetamide (5a5k) compounds has been synthesized and these compounds were characterized with spectral data like IR, NMR and Mass spectroscopy.. All compounds were evaluated in vitro for their efficacy as antimicrobial against Gram positive and Gram negative pathogenic bacterial strains such as S. aureus, B. subtilis, E coli and P. aeruginosa using ciprofloxacin as a standard and fungal strains like C. Albicans and A. fumigatus as compare with standard drug Clotrimazole and Molecular docking study shown all these compounds were having good to excellent correlation binding energy as compare with binding energy of standard drugs. Article Title: 1,2-Phenylene-Incorporated Smallest Expanded Calix[4]pyrrole via One-Step Synthesis of Tetrapyrrane: A Fluorescent Host for Fluoride Ion. Article Snippet: Synthesis of tetrapyrrane 8 from acetone and pyrrole via one-step condensation was achieved for the first time along with a much-improved yield of the tripyrrane 9.. Diborylation of the tetrapyrrane and subsequent “1 + 1” cyclocoupling with 1,2diiodobenzene following the Suzuki protocol generated novel o-phenylene incorporated macrocycle belonging to the smallest mesoexpanded calix[4]pyrrole family.. The latter macrocycle displays exclusive turn-on fluorescence sensing of fluoride ion upon complexation via a unique partial cone conformation supported by DFT analysis in acetonitrile solvent. Article Title: The Baylis–Hillman acetates as a source of ambiphilic molecules: a simple synthesis of 1,3-thiazinane-2-thione frameworks Article Snippet: Accepted Manuscript The Baylis-Hillman Acetates as a Source of Ambiphilic Molecules: A Simple Synthesis of 1,3-Thiazinane-2-thione Frameworks Deevi Basavaiah, Sutanuka Pal, Gorre Veeraraghavaiah, Kishor Chandra Bharadwaj PII: S0040-4020(15)00597-9 DOI: 10.1016/j.tet.2015.04.087 Reference: TET 26690 To appear in: Tetrahedron Received Date: 10 March 2015 Revised Date: 23 April 2015 Accepted Date: 24 April 2015 Please cite this article as: Basavaiah D, Pal S, Veeraraghavaiah G, Bharadwaj KC, The BaylisHillman Acetates as a Source of Ambiphilic Molecules: A Simple Synthesis of 1,3-Thiazinane-2-thione Frameworks, Tetrahedron (2015), doi: 10.1016/j.tet.2015.04.087.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript. |