Table of Contents
How do I connect my ChemDraw to SciFinder?
Answer: Sign in to access SciFinder® as you would normally when using your institution’s proxy and go to a SciFinder Explore page. Once viewing an Explore page, copy the SciFinder proxy access URL shown in the address bar. Return to ChemDraw and click on the Search SciFinder button to re-initiate your search.
What is the difference between SciFinder and SciFinder N?
SciFindern (SFn) is a new and improved version of SciFinder that has an updated interface and search algorithm BUT provides the same great access to data and research users have historically enjoyed. SFn is mobile-friendly, offers more filter options, and includes an “All Search” function similar to Google.
How do you use SciFinder N?
Searching in CAS SciFindern Select the search type: All finds substances, reactions, references, and suppliers that match your query. Enter a text query or click the Draw button to import or draw a structure query. Click the magnifying glass to submit the query.
How do I import a structure into ChemDraw?
In either CAS Draw or ChemDoodle, click the Import/Open icon. Click the Choose File button and navigate to the . mol file you saved to import. Select the file, and then click the Open button The structure will display in the selected drawing tool’s workspace.
What is SciFinder used for?
SciFinder, a resource from the Chemical Abstracts Service (CAS), is a curated database of chemical and bibliographic information that covers several scientific and biomedical fields, with an emphasis on chemistry.
How do I remove duplicates in SciFinder?
Click Preferences in the status bar to view and edit them. Check the box for Remove Duplicate References. SciFinder will automatically remove the duplicate MEDLINE records when a search is conducted.
How do I use SciFinder off campus?
To access SciFinder off campus, you will need to log in twice. Just use this URL to first log in with your KU Online ID as you would for any other library resource that you access from off campus. Then log in with your personal SciFinder login. If you have any problems, please contact me.
Does ChemDraw do reactions?
Chemists can use ChemDraw Professional to draw and submit chemical compound and reaction searches direct to SciFinder, with no more time-consuming cutting and pasting.
Can ChemDraw convert SMILES to structure?
ChemDraw converts between IUPAC systematic names, InChI strings, SMILES strings, and chemical structures. ChemDraw can interpret SMILES and InChI strings as chemical structures.
What does control G do in ChemDraw?
ChemDraw Shortcuts File Commands Command+E toggle fixed angles Command+R Command+G group selected objects Shift+Command+H Shift+Command+G ungroup objects Option+Shift+ Command+H Command+J join selected objects Shift+Command+V.
Does ChemDraw generate SMILES?
SMILES supports an alternate notation for aromatic structures using lowercase letters. ChemDraw generates this type of SMILES string for any structure drawn with explicit aromatic bonds, either by using the Aromatic bond type in the Atom Properties dialog box, or by placing a circle within any ring structure.
What information can you find in SciFinder N *?
CAS SciFindern is your one true source for authoritatively identifying a chemical substance and its related chemical structures, chemical names, regulatory information, and properties, including CAS Registry Numbers®, reaction schemes, step-by-step experimental procedures, detailed conditions, and product yields.
How do I find an author on SciFinder?
Under “References” on the left side of the screen, click “Author Name.” Enter the author’s name, then click search. The more information you provide, the more specific your results will be. Check “Look for alternate spellings of the last name” if you aren’t sure about the spelling of the name.
How do you copy a structure from SciFinder to ChemDraw?
Answer: Try selecting ChemDraw as your clipboard format under SciFinder’s Preferences. To change this or other preferences, click on the “Prefs” button at the top of the SFS window. Click on the Drawing tab to make the ChemDraw selection.
What is Chem Bio Draw?
ChemBioDraw is a software package for drawing chemical structures and creating 3D visualizations of them. The drawing portion of the software package is available for both PCs and Macs.
How does a SciFinder work?
SciFinder, produced by Chemical Abstracts Service (CAS), is the most comprehensive database for the chemical literature, searchable by topic, author, substances by name or CAS Registry Number, OR use the editor to draw chemical structures, substructures, or reactions.
What is the difference between Google Scholar and SciFinder?
SciFinder has the strongest coverage of chemistry and the natural sciences, while Google Scholar has the capability to link citation information to individual references. Although Scopus and Web of Science provide comprehensive citation reports, all databases miss linking to some references included in other databases.
Is SciFinder free?
Accessing SciFinder Create an Account: You will need to create an account (free for UCalgary students, faculty, and staff) to access SciFinder. Once your account is created, you can access it from anywhere with an Internet connection.
How do you write deuterium in SciFinder?
You can search two isotopes: D = deuterium and T= tritium. To begin, click Property. Click the appropriate radio button to select either Experimental or Predicted property.
Why would you use a substructure search in SciFinder?
SciFinder® substructure searching capabilities give you unparalleled substructure access to the world’s largest and most current chemical substance database. By default, substructure searches retrieve exact results, plus substances with additional substitution and/or ring fusion.
How do you get spectra on SciFinder?
Finding Spectra in SciFinder Perform a Substances search for the substance of interest. Click on the substance record. In the record details, look for the “Experimental Spectra” section and open the dropdown menu. Select the tab for proton NMR spectra ( 1 H NMR).
How much does SciFinder cost?
An academic institution or user can subscribe to the task-based, commercial version of SciFinder for $6,500 per year for 310 tasks. Each search is considered a task, and a substructure search counts as four tasks.
How do I use SciFinder free?
To be eligible for free access, scientists must have become unemployed on Jan. 1, 2011 or later, from a U.S., Canadian, or European employer that participates in the SciFinder enterprise-wide pricing program, which provides unlimited access to all scientists across a customer’s organization.
Which database contain the structural information about organometallic compounds?
The Cambridge Structural Database is produced by the Cambridge Crystallographic Data Center (http://www.ccdc.cam.ac.uk/products/csd/). It is a database of x-ray diffraction and neutron diffraction crystal structures of organic and organometallic substances.
