≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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.
Enantioselective oxidation of cis-1,2-cyclohexanedimethanol using 4-acetylamino-2,2,7-trimethyl-10-isopropyl-1-azaspiro[5.5]undecane N-oxyl as a chiral nitroxyl radical via non-electrochemical method has been reported.
It was used in the synthesis of 9-{[(Z)-2(hydroxymethyl)cyclohexyl]methyl}guanine
| Pubchem Sid | 504760845 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504760845 |
| Kanonisches Lächeln | C1CCC(C(C1)CO)CO |
| IUPAC Name | [(1S,2R)-2-(hydroxymethyl)cyclohexyl]methanol |
| InChIKey | XDODWINGEHBYRT-OCAPTIKFSA-N |
| INCHI | 1S/C8H16O2/c9-5-7-3-1-2-4-8(7)6-10/h7-10H,1-6H2/t7-,8+ |
| Isomere SMILES | C1CC[C@H]([C@H](C1)CO)CO |
| Molekulargewicht | 144.21 |
| Beilstein | 6(4)5234 |
| Reaxy-Rn | 2071381 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2071381&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 | Organic oxygen compounds |
| Klasse | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Primary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Hydrocarbon derivative - Primary alcohol - Aliphatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 I2212011 | Certificate of Analysis | Mar 11, 2026 | I133239 |
| I2212010 | Certificate of Analysis | Jun 18, 2024 | I133239 |
| D1813148 | Certificate of Analysis | Oct 13, 2023 | I133239 |
| D1813144 | Certificate of Analysis | Oct 13, 2023 | I133239 |
| Siedepunkt (°C) | 112 °C/0.6 mmHg |
|---|---|
| Schmelzpunkt (°C) | 40 °C |
| Molekulargewicht | 144.210 g/mol |
| XLogP3 | 0.900 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 144.115 Da |
| Monoisotopic Mass | 144.115 Da |
| Topological Polar Surface Area | 40.500 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 81.300 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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 |
