Frequently Asked Questions Live Chat and Frequently Asked Questions are available for this Product. 包装 1, 2.5 L in glass bottle 25, 500 mL in glass bottle
Frequently Asked Questions Live Chat and Frequently Asked Questions are available for this Product. 包装 1, 6×1, 2, 4×2, 2.5, 4×2.5, 4×4 L in glass bottle 20, 200 L in steel drum 500, 6×500 mL in glass bottle
Molecular Biology Reagent Purity: 99+% Used for PCR aqueous phase recovery overlaid with mineral oil.
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• For example of use in the generation of dichlorocarbene under phase-transfer catalysis, see: Org. Synth. Coll., 7, 12 (1990). See also Bromoform, A11904.
• In the presence of base, phenols undergo formylation predominantly in the ortho-position, to give salicylaldehyde derivatives (the Reimer-Tiemann reaction). The mechanism probably involves dichlorocarbene, and yields are generally rather low. For an example, see: Org. Synth. Coll., 3, 463 (1955); review: Org. React., 28, (1982). Improved procedures have been reported: Synth. Commun., 18, 2095 (1988); and, using ultrasound: Synth. Commun., 20, 609 (1990); for an example, see 4-Chlorophenol, A15602.