≥98% 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.
l'alcool 3,5-dinitrobenzyle réagit avec le chlorure de p-toluènesulfonyle et donne le p-toluènesulfonate de 3,5-dinitrobenzyle.
l'alcool 3,5-dinitrobenzyle a été utilisé dans la synthèse de l'alcool 3,5-bis((bezoxycarbonyl)imino)benzyle.
| Pubchem Sid | 488187529 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187529 |
| Sourires canoniques | C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])CO |
| IUPAC Name | (3,5-dinitrophenyl)methanol |
| InChIKey | GPHYIQCSMDYRGJ-UHFFFAOYSA-N |
| INCHI | 1S/C7H6N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-3,10H,4H2 |
| Isomères SMILES | C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])CO |
| WGK Allemagne | 3 |
| Poids moléculaire | 198.13 |
| Reaxy-Rn | 2054388 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2054388&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 | Benzenoids |
| Classe | Benzene and substituted derivatives |
| Subclass | Nitrobenzenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitrobenzenes |
| Alternative Parents | Nitroaromatic compounds Benzyl alcohols Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives Aromatic alcohols |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Nitrobenzene - Benzyl alcohol - Nitroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Alcohol - Hydrocarbon derivative - Organic zwitterion - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 L22071160 | Certificate of Analysis | Sep 07, 2026 | D154155 |
| D23061176 | Certificate of Analysis | Apr 12, 2023 | D154155 |
| F1918168 | Certificate of Analysis | Apr 12, 2023 | D154155 |
| F2326106 | Certificate of Analysis | Apr 12, 2023 | D154155 |
| E2606081 | Certificate of Analysis | Dec 15, 2022 | D154155 |
| Solubilité | Soluble in Methanol |
|---|---|
| Point de fusion (°C) | 89-93°C |
| Poids moléculaire | 198.130 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | 198.028 Da |
| Monoisotopic Mass | 198.028 Da |
| Topological Polar Surface Area | 112.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 211.000 |
| 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 |
