≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
Reactant for:Preparation of vinyloxyboranesDicyclohexyliodoborane (Chx2BI) can be used as a reagent:For the enolboration of esters and tertiary amides to synthesize correspondingZorEenolates.In the stereoselective preparation of β-hydroxy-α-trifluoromethyl carboxylic acids via haloborane-mediated diastereoselective aldol addition of aldehydes with trifluoropropanoic acid.In the total synthesis of pordamacrine A, and trocheliophorolide D.
| Sonrisas canónicas | B(C1CCCCC1)(C2CCCCC2)I |
|---|---|
| IUPAC Name | dicyclohexyl(iodo)borane |
| InChIKey | RWFGGTOYIFQXAO-UHFFFAOYSA-N |
| INCHI | 1S/C12H22BI/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2 |
| Isómeros SMILES | B(C1CCCCC1)(C2CCCCC2)I |
| Peso molecular | 304.02 |
| Reaxy-Rn | 3233943 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3233943&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organometallic compounds |
| Clase | Organometalloid compounds |
| Subclass | Organoboron compounds |
| Intermediate Tree Nodes | Alkylboranes |
| Direct Parent | Alkylhaloboranes |
| Alternative Parents | Organic metalloid salts Dialkylboranes Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Alkylhaloborane - Dialkylborane - Organic metalloid salt - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alkylhaloboranes. These are organoboron compounds with the general formula RBX2 or R2BX (R=alkyl, X=halogen). |
| External Descriptors | Not available |
| Peso molecular | 304.020 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 304.086 Da |
| Monoisotopic Mass | 304.086 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 142.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
