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4-Chlorobenzaldehyde (o-Chlorobenzaldehyde) is an organic compound with the formula ClC 5 H 4 CHO. It is one of three isomeric monochlorinated benzaldehydes . Preparation
Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.
Be(NO 3) 2: beryllium nitrate: 13597–99–4 Be(NO 3) 2 •4H 2 O: beryllium nitrate tetrahydrate: 13510–48–0 Be(NO 3) 2 •3H 2 O: beryllium nitrate trihydrate: 7787–55–5 BeO: beryllium oxide: 1304–56–9 Be(OH) 2: beryllium hydroxide: 13327–32–7 BeS: beryllium sulfide: 13598–22–6 BeSO 4: beryllium sulfate: 13510–49–1 ...
1-4 hours Flu-like, also eye, nose, and throat irritation, and chest discomfort, or no symptoms Phosgene Gas: colorless Odor: decaying fruit, fresh-cut grass, 1-4 hours; small doses, 24-48 hours Burning eyes, sore throat, dry cough, and chest tightness
4-Chloroaniline is used in the industrial production of pesticides, drugs, and dyestuffs. It is a precursor to the widely used antimicrobial and bacteriocide chlorhexidine and is used in the manufacture of pesticides, including pyraclostrobin, anilofos, monolinuron, and chlorphthalim.
[4] Inorganic chloramines are produced by the reaction of ammonia and hypochlorous acid or chlorine . An urban legend claims that mixing household bleach (aqueous sodium hypochlorite ) with ammonia-based cleaners releases chlorine gas or mustard gas ; in reality, the gas produced by the reaction is a mixture of inorganic chloramines.
CAS number; C 4 Br 2: dibromobutadiyne: 36333-41-2 C 4 Ce: cerium tetracarbide: 12151-79-0 C 4 ClF 7 O: heptafluorobutyryl chloride: 375-16-6 C 4 Cl 2 F 4 O 2: tetrafluorosuccinyl chloride: 356-15-0 C 4 Cl 2 F 4 O 3: chlorodifluoroacetic anhydride: 2834-23-3 C 4 Cl 2 O 4 Rh 2: dirhodium tetracarbonyl dichloride: 14523-22-9 C 4 Cl 3 CoO 4 Si ...
H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.