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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. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    The deliberate protodeboronation of boronic acids (and derivatives) have been applied to some synthetic procedures, such as the installation of a stereospecific proton at chiral centers, [2] and also in purification procedures, such as the removal of unwanted regioisomeric boronic acid by-products.

  5. Carbamate - Wikipedia

    en.wikipedia.org/wiki/Carbamate

    h 2 nco − 2 + h 2 o ⇌ nh + 4 + co 2− 3 Calcium carbamate is soluble in water, whereas calcium carbonate is not. Adding a calcium salt to an ammonium carbamate/carbonate solution will precipitate some calcium carbonate immediately, and then slowly precipitate more as the carbamate hydrolyzes.

  6. Pyrimidine metabolism - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine_metabolism

    Products 1 carbamoyl phosphate synthetase II [2] carbamoyl phosphate: This is the regulated step in the pyrimidine biosynthesis in animals. 2 aspartic transcarbamoylase (aspartate carbamoyl transferase) [2] carbamoyl aspartic acid: The phosphate group is replaced with Aspartate. This is the regulated step in the pyrimidine biosynthesis in ...

  7. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    The general structure of a boronic acid, where R is a substituent.. A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1]

  8. Trump's Mexican tariffs threaten to make life more difficult ...

    www.aol.com/trumps-tariffs-hard-automakers-mdash...

    Donald Trump has vowed to hit Mexico with a 25% tariff, which would affect automakers including Tesla. Tesla announced plans in 2023 for a $10 billion factory in Mexico, whose future remains ...

  9. Hydantoin - Wikipedia

    en.wikipedia.org/wiki/Hydantoin

    Hydantoin, or glycolylurea, is a heterocyclic organic compound with the formula CH 2 C(O)NHC(O)NH. It is a colorless solid that arises from the reaction of glycolic acid and urea.