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  2. List of chemical databases - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_databases

    Chemexper Chemical Directory catalogue chemicals CASno Structure SMILES "ChemExper". Chemxpert Database Chemxpert Chemical Database small molecules database buyers,suppliers "ChemxpertDB". 10,00000 Chemical Book East West University: commercially available compounds CASno, suppliers, properties "Chemical Book". 200,000 Chemical Register

  3. Template:Calendar - Wikipedia

    en.wikipedia.org/wiki/Template:Calendar

    Display a year or month calendar Template parameters [Edit template data] Parameter Description Type Status Year year the ordinal year number of the calendar Default current Number suggested Month month whether to display a single month instead of a whole year, and which one Default empty Example current, next, last, 1, January String suggested Show year show_year whether to display the year ...

  4. 4,4'-Methylenebis (2-chloroaniline) - Wikipedia

    en.wikipedia.org/wiki/4,4'-Methylenebis(2...

    4,4′-Methylenebis(2-chloroaniline) (also known as MOCA, MBOCA, and bisamine) is a substance used as a curing agent in polyurethane production. [3] MOCA is an aromatic amine which is structurally similar to benzidine, a known human bladder carcinogen.

  5. Thiocarbonyldiimidazole - Wikipedia

    en.wikipedia.org/wiki/Thiocarbonyldiimidazole

    Download as PDF; Printable version; In other projects ... Chemical formula. C 7 H 6 N 4 S: Molar mass: ... This page was last edited on 11 August 2024, ...

  6. TCI - Wikipedia

    en.wikipedia.org/wiki/TCI

    TCI. 8 languages. Deutsch; ... Download as PDF; Printable version; In other projects ... This page was last edited on 27 April 2024, at 11:27 (UTC).

  7. 1,3-Dimethyl-2-imidazolidinone - Wikipedia

    en.wikipedia.org/wiki/1,3-Dimethyl-2-imidazolidinone

    In 1940 Du Pont applied for a patent on acetylene storage in many polar organic solvents, one of which was 1,3-dimethyl-2-imid azolidone. [5] The company filed another patent on a method of synthesizing the same compound, albeit called s-dimethylethyleneurea, in 1944.