3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile
In the title molecule, C14H16N2O, the cyclohexane ring adopts a chair conformation. The oxime group has an equatorial orientation. The cyano group and the methyl group have axial and equatorial orientations, respectively. The phenyl ring has an equatorial orientation. The structure is stabilized by...
Gespeichert in:
Veröffentlicht in: | Acta crystallographica. Section E, Structure reports online Structure reports online, 2007-06, Vol.63 (6), p.o2780-o2780 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | o2780 |
---|---|
container_issue | 6 |
container_start_page | o2780 |
container_title | Acta crystallographica. Section E, Structure reports online |
container_volume | 63 |
creator | Thiruvalluvar, A. Subramanyam, M. Mohan, R. T. Sabapathy Kamatchi, S. Murugavel, K. |
description | In the title molecule, C14H16N2O, the cyclohexane ring adopts a chair conformation. The oxime group has an equatorial orientation. The cyano group and the methyl group have axial and equatorial orientations, respectively. The phenyl ring has an equatorial orientation. The structure is stabilized by intermolecular O—H...N hydogen bonds and intramolecular C—H...O interactions. |
doi_str_mv | 10.1107/S1600536807020892 |
format | Article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1107_S1600536807020892</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>AYE2AT2282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2952-ba4bfec1d6008943293d0adaf45df6e120f2e03c2334725e09c4c05b01a9be833</originalsourceid><addsrcrecordid>eNqFUMtKxEAQHETBdfUD_IhoT08myRzDshphwYPrwVOYTHpIJI9lsuDOzU_wG_0SJ-weBA8eiq4uupqiGLvlcMc5pPcvPAGQIskgBYRM4RlbzFI0a-e_-CW7mqZ3AJ6kyBesEN-fX4Wv3Xjwbd8OY1h5QE_7xneByIBdQ4PvjDfd2NBBD3Q6MtpV49DuXdvRNbuwupvo5jSX7PVhvV0V0eb58WmVbyKDSmJU6biyZHgd8mQqFqhEDbrWNpa1TYgjWCQQBoWIU5QEysQGZAVcq4oyIZaMH_8aN06TI1vuXNtr50sO5VxF-aeK4FFHz0cI6v83lPnbGvMtYobiB4E5aH8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Free Full-Text Journals in Chemistry</source><creator>Thiruvalluvar, A. ; Subramanyam, M. ; Mohan, R. T. Sabapathy ; Kamatchi, S. ; Murugavel, K.</creator><creatorcontrib>Thiruvalluvar, A. ; Subramanyam, M. ; Mohan, R. T. Sabapathy ; Kamatchi, S. ; Murugavel, K.</creatorcontrib><description>In the title molecule, C14H16N2O, the cyclohexane ring adopts a chair conformation. The oxime group has an equatorial orientation. The cyano group and the methyl group have axial and equatorial orientations, respectively. The phenyl ring has an equatorial orientation. The structure is stabilized by intermolecular O—H...N hydogen bonds and intramolecular C—H...O interactions.</description><identifier>ISSN: 1600-5368</identifier><identifier>EISSN: 1600-5368</identifier><identifier>DOI: 10.1107/S1600536807020892</identifier><language>eng</language><publisher>5 Abbey Square, Chester, Cheshire CH1 2HU, England: Blackwell Publishing Ltd</publisher><ispartof>Acta crystallographica. Section E, Structure reports online, 2007-06, Vol.63 (6), p.o2780-o2780</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2952-ba4bfec1d6008943293d0adaf45df6e120f2e03c2334725e09c4c05b01a9be833</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1107%2FS1600536807020892$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1107%2FS1600536807020892$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids></links><search><creatorcontrib>Thiruvalluvar, A.</creatorcontrib><creatorcontrib>Subramanyam, M.</creatorcontrib><creatorcontrib>Mohan, R. T. Sabapathy</creatorcontrib><creatorcontrib>Kamatchi, S.</creatorcontrib><creatorcontrib>Murugavel, K.</creatorcontrib><title>3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile</title><title>Acta crystallographica. Section E, Structure reports online</title><description>In the title molecule, C14H16N2O, the cyclohexane ring adopts a chair conformation. The oxime group has an equatorial orientation. The cyano group and the methyl group have axial and equatorial orientations, respectively. The phenyl ring has an equatorial orientation. The structure is stabilized by intermolecular O—H...N hydogen bonds and intramolecular C—H...O interactions.</description><issn>1600-5368</issn><issn>1600-5368</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFUMtKxEAQHETBdfUD_IhoT08myRzDshphwYPrwVOYTHpIJI9lsuDOzU_wG_0SJ-weBA8eiq4uupqiGLvlcMc5pPcvPAGQIskgBYRM4RlbzFI0a-e_-CW7mqZ3AJ6kyBesEN-fX4Wv3Xjwbd8OY1h5QE_7xneByIBdQ4PvjDfd2NBBD3Q6MtpV49DuXdvRNbuwupvo5jSX7PVhvV0V0eb58WmVbyKDSmJU6biyZHgd8mQqFqhEDbrWNpa1TYgjWCQQBoWIU5QEysQGZAVcq4oyIZaMH_8aN06TI1vuXNtr50sO5VxF-aeK4FFHz0cI6v83lPnbGvMtYobiB4E5aH8</recordid><startdate>200706</startdate><enddate>200706</enddate><creator>Thiruvalluvar, A.</creator><creator>Subramanyam, M.</creator><creator>Mohan, R. T. Sabapathy</creator><creator>Kamatchi, S.</creator><creator>Murugavel, K.</creator><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200706</creationdate><title>3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile</title><author>Thiruvalluvar, A. ; Subramanyam, M. ; Mohan, R. T. Sabapathy ; Kamatchi, S. ; Murugavel, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2952-ba4bfec1d6008943293d0adaf45df6e120f2e03c2334725e09c4c05b01a9be833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thiruvalluvar, A.</creatorcontrib><creatorcontrib>Subramanyam, M.</creatorcontrib><creatorcontrib>Mohan, R. T. Sabapathy</creatorcontrib><creatorcontrib>Kamatchi, S.</creatorcontrib><creatorcontrib>Murugavel, K.</creatorcontrib><collection>CrossRef</collection><jtitle>Acta crystallographica. Section E, Structure reports online</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thiruvalluvar, A.</au><au>Subramanyam, M.</au><au>Mohan, R. T. Sabapathy</au><au>Kamatchi, S.</au><au>Murugavel, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile</atitle><jtitle>Acta crystallographica. Section E, Structure reports online</jtitle><date>2007-06</date><risdate>2007</risdate><volume>63</volume><issue>6</issue><spage>o2780</spage><epage>o2780</epage><pages>o2780-o2780</pages><issn>1600-5368</issn><eissn>1600-5368</eissn><abstract>In the title molecule, C14H16N2O, the cyclohexane ring adopts a chair conformation. The oxime group has an equatorial orientation. The cyano group and the methyl group have axial and equatorial orientations, respectively. The phenyl ring has an equatorial orientation. The structure is stabilized by intermolecular O—H...N hydogen bonds and intramolecular C—H...O interactions.</abstract><cop>5 Abbey Square, Chester, Cheshire CH1 2HU, England</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1107/S1600536807020892</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1600-5368 |
ispartof | Acta crystallographica. Section E, Structure reports online, 2007-06, Vol.63 (6), p.o2780-o2780 |
issn | 1600-5368 1600-5368 |
language | eng |
recordid | cdi_crossref_primary_10_1107_S1600536807020892 |
source | Wiley Online Library Journals Frontfile Complete; Free Full-Text Journals in Chemistry |
title | 3‐Hydroxyimino‐1‐methyl‐5‐phenylcyclohexane‐1‐carbonitrile |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T22%3A45%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=3%E2%80%90Hydroxyimino%E2%80%901%E2%80%90methyl%E2%80%905%E2%80%90phenylcyclohexane%E2%80%901%E2%80%90carbonitrile&rft.jtitle=Acta%20crystallographica.%20Section%20E,%20Structure%20reports%20online&rft.au=Thiruvalluvar,%20A.&rft.date=2007-06&rft.volume=63&rft.issue=6&rft.spage=o2780&rft.epage=o2780&rft.pages=o2780-o2780&rft.issn=1600-5368&rft.eissn=1600-5368&rft_id=info:doi/10.1107/S1600536807020892&rft_dat=%3Cwiley_cross%3EAYE2AT2282%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |