C4H8O, Empirical Formula (Hill Notation): C5H11BN2, Synonym: BH3–THF’s relative stability makes it a convenient way to use extremely toxic and flammable diborane. Diversity in Chemistry Awards pricing. NACRES NA.22 Now offered virtually. 1155 Sixteenth Street, NW, Washington, DC 20036, USA | service@acs.org | 1-800-333-9511 (US and Canada) | 614-447-3776 (outside North America), Copyright © 2020 American Chemical Society. In the past, borane molecules were often labeled "electron-deficient" because of their multicenter bonding (in which a pair of bonding electrons links more than two atoms, as in 3-center-2-electron bonds); this was done in order to distinguish such molecules from hydrocarbons and other classically bonded compounds. In 2018, the US Environmental Protection Agency reported that it was a low risk to human health and the environment, but this was disputed by a scientific advisory committee and environmental groups. The agency ordered manufacturer Sun Chemical and importer BASF to provide additional data concerning worker exposure. —Ed. Learn more about this molecule from CAS, the most authoritative and comprehensive source for chemical information. Borane tetrahydrofuran complex solution, 1.0 M in THF, contains 0.005 M 1,2,2,6,6-pentamethylpiperidine as stabilizer. See our Browser Support/Compatibility page for supported browsers list. The complex is commercially available but can also be generated by the dissolution of diborane in THF. This molecule was suggested by a reader. It reacts with olefins to add the BH 2 functional group. H. 11. The molecule can be notable for its current or historical importance or for any quirky reason. Borane tetrahydrofuran. Borane tetrahydrofuran complex solution, 1.0 M in THF, contains 0.005 M N-Isopropyl-N-methyl-tert-butylamine as stabilizer. However, this usage is incorrect, as most boranes and related clusters such as carboranes are actually … ACS-Hach Programs Company Identification: Acros Organics N.V. One Reagent Lane Fair Lawn, NJ 07410 For information in North America, call: 800-ACROS-01 For emergencies in the US, call CHEMTREC: 800-424-9300 ACS is committed to helping combat the global COVID-19 pandemic with initiatives and free resources. In particular, it reacts violently with water to produce copious amounts of hydrogen. Collaborate with scientists in your field of chemistry and stay current in your area of specialization. Structure. For your security, this online session is about to end due to inactivity. Find awards and scholarships advancing diversity in the chemical sciences. Reactions: Chemistry Science Videos & Infographics Learn about financial support for future and current high school chemistry teachers. Molecular Weight 85.94 . Technical Divisions Launch and grow your career with career services and resources. © 2020  Merck KGaA, Darmstadt, Germany and/or its affiliates. MDL number MFCD00012429. 100-200 mesh, extent of labeling: 0.8-1.0 mmol/g loading, 1 % cross-linked with divinylbenzene. *Hazard information is available only for the article of commerce, typically a 1 M solution in THF. 1.0 M in THF, contains 0.005 M N -Isopropyl- N -methyl- tert -butylamine as stabilizer, 97.5 atom % D (mimimum) Sigma-Aldrich. B-Isopinocampheyl-9-borabicyclo[3.3.1]nonane solution. Linear Formula BH 3 OC 4 H 8. As an example, BH3–THF can be distilled without decomposing. Promoting excellence in science education and outreach. Borane tetrahydrofuran complex solution 1.0 M in THF CAS Number 14044-65-6. >. Advance your career with professional development courses. Explore the interesting world of science with articles, videos and more. 2723981. ACS Professional Education Explore chemistry education resources by topic that support distance learning. If you do not respond, everything you entered on this page will be lost and you will have to login again. Learn More. We present almost all of the molecules suggested by our readers. Chemistry at Home If you have a molecule you would like us to consider, please send an e-mail to motw@acs.org. C4H11BO. It can be used to reduce carboxylic acids to alcohols or nitriles to primary amines. Beilstein/REAXYS Number 3668402 . The preparation of borane carbonyl, BH 3 (CO), played an important role in exploring the chemistry of boranes, as it indicated the likely existence of the borane molecule. Explanation of pictograms. Find Similar Structures. American Association of Chemistry Teachers, Reactions: Chemistry Science Videos & Infographics, Chemicals which, in contact with water, emit flammable gases, category 1, H260—In contact with water releases flammable gases that may ignite spontaneously, Serious eye damage/eye irritation, category 1, Specific target organ toxicity, single exposure, respiratory system, category 3. Uncover the Chemistry in Everyday Life, Recognizing and celebrating excellence in chemistry and celebrate your achievements. Network with colleagues and access the latest research in your field. Thank you! It can be used to reduce carboxylic acids to alcohols or nitriles to primary amines. Under standard conditions, borane dimerizes to produce the more electronically stable diborane. | Privacy. In the past month, EPA revised its assessment, stating that PV29 exposure poses unreasonable risks to workers under certain conditions. Site Use Terms All Rights Reserved. 1. I’m a handy compound to tame a useful reagent. MSDS Name: Borane-tetrahydrofuran complex, 1M solution in THF, stabilized Catalog Numbers: AC175080000, AC175081000, AC175088000 Synonyms: None known. Alkyl- or arylboranes formed in this way can further react with unsaturated compounds such as olefins, imines, ketones, and alkynes (the hydroboration reaction) to make useful boron-containing intermediates. Average mass 85.940 Da. PubChem Substance ID 24850560. The electrostatic attraction between the components is not as strong as a covalent bond; but in many cases it is sufficient to make the complex behave as a covalent compound. Charge-transfer complexes such as BH3–THF form when a Lewis base (THF in this case) “donates” its unshared electron pair to an electron-deficient Lewis acid such as borane. Explore Career Options Borane tetrahydrofuran. Borane - tetrahydrofuran (1:1) Molecular Formula C. 4. B-Isopinocampheyl-9-borabicyclo[3.3.1]nonane, Empirical Formula (Hill Notation): C18H31B, Synonym: Molecular Formula. Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. 15. Boranes is the name given to the class of synthetic hydrides of boronwith generic formula BxHy. Borane–tetrahydrofuran (BH 3 –THF) is a charge-transfer complex that is a useful surrogate for diborane 1 in organic synthesis. It is a perylene-based compound that is used in a wide range of coloring applications, including paints, inks, paper, carpets, solar cells, and drugs. 667714. Trihydridoboron, also known as borane or borine, is an unstable and highly reactive molecule with the chemical formula BoronB H3. Monoisotopic mass 86.090294 Da. BO. ChemSpider ID 2006157. 2-Picoline borane complex, Empirical Formula (Hill Notation): C15H18BOPS, Synonym: Find a chemistry community of interest and connect on a local and global level. Synonyms. 1-Bromo-N,N,N′,N′-tetramethylboranediamine, Empirical Formula (Hill Notation): C12H26BN, Empirical Formula (Hill Notation): C6H18BN, Synonym: Learn how ACS can help you stay ahead in the world of chemistry. As a result, BH3–THF is normally sold as a 1 M (≈10 wt%) solution in THF. And thank you for your interest in Molecule of the Week! A practical route to this is the oxidation of sodium borohydride with iodine in THF. Reproduction of any materials from the site is strictly forbidden without permission. It reacts with olefins to add the BH2 functional group. Borane-tetrahydrofuran complex, BTHF-1M in THF contains 0.005M sodium borohydride as stabilizer.