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  2. Carbamic acid - Wikipedia

    en.wikipedia.org/wiki/Carbamic_acid

    Carbamic acid is a planar molecule. [3]The H 2 N− group of carbamic acid, unlike that of most amines, cannot be protonated to an ammonium group H 3 N + −.The zwitterionic form H 3 N + −COO − is very unstable and promptly decomposes into ammonia and carbon dioxide, [6] yet there is a report of its detection in ices irradiated with high-energy protons.

  3. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  4. Carbamate - Wikipedia

    en.wikipedia.org/wiki/Carbamate

    In water solutions, the carbamate anion slowly equilibrates with the ammonium NH + 4 cation and the carbonate CO 2− 3 or bicarbonate HCO − 3 anions: [3] [4] [5] H 2 NCO − 2 + 2 H 2 O ⇌ NH + 4 + HCO − 3 + OH − H 2 NCO − 2 + H 2 O ⇌ NH + 4 + CO 2− 3. Calcium carbamate is soluble in water, whereas calcium carbonate is not.

  5. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    Basic heteroaromatic boronic acids (boronic acids that contain a basic nitrogen atom, such as 2-pyridine boronic acid) display additional protodeboronation mechanisms. [4] A key finding shows the speciation of basic heteroaromatic boronic acids to be analogous to that of simple amino acids , with zwitterionic species forming under neutral pH ...

  6. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    Removal of the BOC group in amino acids can be accomplished with strong acids such as trifluoroacetic acid in dichloromethane, or with HCl in methanol. [ 2 ] [ 3 ] [ 4 ] A complication may be the tendency of the t -butyl cation intermediate to alkylate other nucleophiles; scavengers such as anisole or thioanisole may be used.

  7. 5-Ethyl-2-methylpyridine - Wikipedia

    en.wikipedia.org/wiki/5-Ethyl-2-methylpyridine

    5-Ethyl-2-methylpyridine is an organic compound with the formula (C 2 H 5)(CH 3)C 5 H 3 N. One of several isomeric pyridines with this formula, this derivative is of interest because it is efficiently prepared from simple reagents and it is a convenient precursor to nicotinic acid, a form of vitamin B 3. 5-Ethyl-2-methylpyridine is a colorless ...

  8. Surge in walking pneumonia affects these high-risk groups ...

    www.aol.com/surge-walking-pneumonia-affects-high...

    Between March 31 and Oct. 5 of this year, the percentage of cases grew from 1% to 7.2% among children ages 2 to 4, and from 3.6% to 7.4% among those ages 5 to 17, the agency stated.

  9. Perfluoroalkyl carboxylic acids - Wikipedia

    en.wikipedia.org/.../Perfluoroalkyl_carboxylic_acids

    Trifluoroacetic acid is a widely employed acid, used for example in the synthesis of peptides.Its esters are useful in analytical chemistry. Longer-chain perfluoroalkyl carboxylic acids, e.g. with five to nine carbons, are useful fluorosurfactants and emulsifiers used in the production of polytetrafluoroethylene (Teflon) and related fluoropolymers.