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Cycloheptene is a 7-membered cycloalkene with a flash point of −6.7 °C. It is a raw material in organic chemistry and a monomer in polymer synthesis. Cycloheptene can exist as either the cis - or the trans -isomer.
REFPROP is a software program for the prediction of thermophysical properties of fluids, developed by the National Institute of Standards and Technology (NIST). [1] [2] [3]The primary component of REFPROP is an equation of state for each implemented fluid.
4-methylpent-2-yne; 3,3-dimethylbut-1-yne This page was last edited on 22 May 2021, at 18:45 (UTC). Text is available under the Creative Commons Attribution ...
N,6-Dimethylhept-5-en-2-amine. CAS Number: 503-01-5 ... [1] [2] Along with paracetamol and dichloralphenazone, it is one of the constituents of Amidrine. Chemistry
Group transfer reactions can be divided into two distinct subcategories: the ene reaction and the diimide reduction. [2] Group transfer reactions have diverse applications in various fields, including protein adenylation, biocatalytic and chemoenzymatic approaches for chemical synthesis, and strengthening skim natural rubber latex.
Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...
4-Methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene (MBP) is a metabolite of bisphenol A (BPA). [1] MBP has potent estrogenic activity in vitro and in vivo, up to thousandfold stronger than BPA. [2] It may also play a role in neuronal cell apoptosis [3] and may increase risk for several forms of cancer. [4] [5] [6]
Dihydrotachysterol (DHT) is a synthetic vitamin D analog activated in the liver that does not require renal hydroxylation like vitamin D 2 (ergocalciferol) and vitamin D 3 (cholecalciferol). DHT has a rapid onset of action (2 hours), a shorter half-life, and a greater effect on mineralization of bone salts than does vitamin D. [ 1 ]