Iupac name of chloroform

  1. chloroform (CHEBI:35255)
  2. Chloroform, 99+%, extra pure, stabilized with amylene, Thermo Scientific Chemicals, Quantity: 1 L
  3. Registration Dossier
  4. Name generator
  5. 1.3: Functional groups and organic nomenclature
  6. What is the structure and uses of chloroform?


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chloroform (CHEBI:35255)

A substance used in a thermodynamic heat pump cycle or refrigeration cycle that undergoes a phase change from a gas to a liquid and back. Refrigerants are used in air-conditioning systems and freezers or refrigerators and are assigned a "R" number (by ASHRAE - formerly the American Society of Heating, Refrigerating and Air Conditioning Engineers), which is determined systematically according to their molecular structure. A class of drugs producing both physiological and psychological effects through a variety of mechanisms involving the central nervous system. ChEBI Ontology Outgoing chloroform ( has role carcinogenic agent ( chloroform ( has role central nervous system drug ( chloroform ( has role inhalation anaesthetic ( chloroform ( has role non-polar solvent ( chloroform ( has role refrigerant ( chloroform ( is a chloromethanes ( chloroform ( is a one-carbon compound ( Incoming trichloromethyl group ( is substituent group from chloroform (

Chloroform, 99+%, extra pure, stabilized with amylene, Thermo Scientific Chemicals, Quantity: 1 L

CAS 67-66-3, 513-35-9 Molecular Formula CHCl3 Molecular Weight (g/mol) 119.37 MDL Number MFCD00000826 InChI Key HEDRZPFGACZZDS-UHFFFAOYSA-N Synonym trichloromethane, formyl trichloride, methane, trichloro, trichloroform, methane trichloride, methenyl trichloride, methyl trichloride, trichlormethan, chloroforme, cloroformio PubChem CID ChEBI IUPAC Name chloroform SMILES ClC(Cl)Cl This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals. Melting Point -63.0°C Assay Percent Range 99+% Linear Formula CHCl 3 Merck Index 15, 2142 Solubility Information Solubility in water: 8g/L (20°C). Other solubilities: miscible with alcohol, benzene, ether, petr.ether,, carbon tetrachloride, carbon disulfide and oils., soluble in acetone. Formula Weight 119.38 Percent Purity ≥99% Grade Extra Pure Density 1.4800g/mL Boiling Point 61.0°C Quantity 1 L Packaging Glass Bottle Physical Form Liquid Residue after Evaporation 0.002% max. Specific Gravity 1.48 Viscosity 0.56 mPa.s (20°C) Water 0.1% max. (K.F.) Chemical Name or Material Chloroform, Stabilized with amylene GHS P Statement Causes skin irritation. Causes serious eye irritation. Harmful if swallowed. Toxic if inhaled. Suspected of causing cancer. May cause drowsiness or dizzin...

Registration Dossier

• General information • Classification & Labelling & PBT assessment • Manufacture, use & exposure • Physical & Chemical properties • Environmental fate & pathways • Ecotoxicological information • Toxicological information • Analytical methods • Guidance on safe use • Assessment reports • Reference substances • • Toxicokinetics, metabolism and distribution • • • • Acute Toxicity • • • • • • Irritation / corrosion • • • • Sensitisation • • • • Repeated dose toxicity • • • • • • Genetic toxicity • • • • • Toxicity to reproduction • • • • • Specific investigations • • • • • • Exposure related observations in humans • • • • • • • • Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice. Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

Name generator

Name generator Name generator Since version 4.1.7, Marvin contains a IUPAC name generator for the computation of the IUPAC name of any compound. When possible, the generated name conforms to the Importing IUPAC names is available from version 5.1. You can generate either the "Traditional Name" or the "Preferred IUPAC Name" of the molecules; you can change between these options in the IUPAC Name Options panel. By default, the "Preferred IUPAC Name" option is set. If the traditional name cannot be generated, the preferred IUPAC Name will be generated automatically. By default, molecules are handled separately if more than one molecule are drawn in the sketcher. However, sometimes a single molecule consists of more fragments (e.g. salt molecules), where the fragments should be treated as one molecule. This can be reached by switching off the "Single fragment mode" option in the IUPAC Name Options panel. The snapshot below shows a molecule taken from the IUPAC specification, with its name computed by Marvin. The contents of the text field can be copied to the clipboard by Ctrl+C, the structure field offers a context menu from MarvinView. The next snapshot below shows a functionality that is available from version 5.0: the IUPAC name can be inserted into the sketch, and it changes with the structure dynamically. This functionality is available from the Insert menu by selecting the IUPAC Name option. Features Supported nomenclatures include: • Chains, Monocycles • Retained/tradi...

1.3: Functional groups and organic nomenclature

[ "article:topic", "alkynes", "alkanes", "amines", "ethers", "nomenclature", "authorname:soderbergt", "nitriles", "alkenes", "aromatics", "alcohols", "showtoc:no", "Functional Groups", "phosphates", "thiols", "sulfides", "license:ccbyncsa", "aldehydes", "ketones", "imines", "abbreviated structures", "haloalkanes", "phenols", "licenseversion:40", "source@https://digitalcommons.morris.umn.edu/chem_facpubs/1/" ] https://chem.libretexts.org/@app/auth/3/login?returnto=https%3A%2F%2Fchem.libretexts.org%2FBookshelves%2FOrganic_Chemistry%2FBook%253A_Organic_Chemistry_with_a_Biological_Emphasis_v2.0_(Soderberg)%2F01%253A_Introduction_to_Organic_Structure_and_Bonding_I%2F1.03%253A_Functional_groups_and_organic_nomenclature \( \newcommand\) • • • • • • • • • • • • • • • • Functional groups are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms. The structure of capsaicin, the compound discussed in the beginning of this chapter, incorporates several functional groups, labeled in the figure below and explained throughout this section. As we progress in our study of organic chemistry, it will become extremely important to be able to quickly recognize the most common functional groups, because they are the key structural elements that define how organic molecules react. For now, we will only worry about drawing and recognizing each functional group, as depicted by Lewis and line structures. Much of the remainder of your stud...

What is the structure and uses of chloroform?

Table of Contents • • • • • • • • What is the structure and uses of chloroform? Chloroform is an organic chemical compound initially employed as an ideal anesthetic. It was first prepared in 1831. The chemical formula is CHCl3. It is colourless, sweet smelling dense liquid produced in large scale. What is the structure of a chemical formula? Structural formulas identify the location of chemical bonds between the atoms of a molecule. A structural formula consists of symbols for the atoms connected by short lines that represent chemical bonds—one, two, or three lines standing for single, double, or triple bonds, respectively. How is CHCl3 formed? Chloroform (CHCl3) is made by taking methane adding chlorine and then heating the compound up until between 400 and 500 degrees Celsius. The products formed are: chloromethane, dichloromethane, chloroform, and carbon tetrachloride. They are then separated by distillation. READ ALSO: Why was Thessalonica an important city? What is the structure of bromoform? CHBr3 Bromoform/Formula What is the Iupac name of chloroform? Trichloromethane Chloroform/IUPAC ID What are the chemical properties of chloroform? Chloroform is a colorless, volatile, liquid derivative of trichloromethane with an ether-like odor. • Chloroform appears as a clear colorless liquid with a characteristic odor. • Chloroform is a colorless liquid with a pleasant, nonirritating odor and a slightly sweet taste. How do you name chemical structures? Summary • A molecular co...

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