When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. 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.

  3. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  4. 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]

  5. Category:Boronic acids - Wikipedia

    en.wikipedia.org/wiki/Category:Boronic_acids

    Phenylboronic acid; Z. ZB716 This page was last edited on 27 March 2013, at 09:31 (UTC). Text is available under the Creative Commons Attribution ...

  6. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    They reported the reaction of phenylboronic acid in water (140-150 °C) to afford the protodeboronated product, benzene, after 40 hours. Initial synthetic applications of protodeboronation were found alongside the discovery of the hydroboration reaction, in which sequential hydroboration-protodeboronation reactions were used to convert alkynes ...

  7. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    4-Formylphenyl boronic acid crystallizes in colorless needles [1] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [3] and readily forms dimers and cyclic trimeric anhydrides, which complicate purification and tend to protodeboronize, a secondary reaction that occurs frequently in the Suzuki coupling, with ...

  8. Risk and Safety Statements - Wikipedia

    en.wikipedia.org/wiki/Risk_and_Safety_Statements

    The R/S statement code for fuming hydrochloric acid (37%): R: 34-37 S: 26-36-45. The corresponding English language phrases: Risks R: 34 Causes burns R: 37 Irritating to the respiratory system. Safety S: 26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S: 36 Wear suitable protective clothing.

  9. Hazardous Materials Identification System - Wikipedia

    en.wikipedia.org/wiki/Hazardous_Materials...

    An example of a HMIS III label for Diesel fuel.. The Hazardous Materials Identification System (HMIS) is a proprietary numerical hazard rating that incorporates the use of labels with color bars developed by the American Coatings Association as a compliance aid for the OSHA Hazard Communication (HazCom) Standard.