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C 10 H 6 Cl 2: dichloro naphthalene: 2050-69-3 C 10 H 6 N 2 OS 2: quinomethionate: 2439-01-2 C 10 H 6 N 2 O 8 S: flavianic acid: 483-84-1 C 10 H 6 N 4 O 2: alloxazine: 490-59-5 C 10 H 6 O 3: phenylmaleic anhydride: 36122-35-7 C 10 H 7 Cl 2 NO: chloro quinaldol: 72-80-0 C 10 H 7 Cl 2 N 3 O: anagrelide: 68475-42-3 C 10 H 7 Cl 5 O: tridiphane ...
Organic carbon compounds are far more numerous than inorganic carbon compounds. In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is ...
1.557 454 318 575 50 × 10 20: 3.373 536 543 484 52 × 10 23: C 55 H 112: n-pentapentacontane: 56 4.191 495 711 934 12 × 10 20: 1.060 278 034 376 26 × 10 24: C 56 H 114: n-hexapentacontane: 57 1.128 939 578 361 33 × 10 21: 3.335 014 088 191 92 × 10 24: C 57 H 116: n-heptapentacontane: 58 3.043 043 571 906 83 × 10 21: 1.049 801 595 284 36 ...
The interconversion of AMP and IMP occurs as part of the purine nucleotide cycle. [3] GMP is formed by the inosinate oxidation to xanthylate (XMP), and afterwards adds an amino group on carbon 2. Hydrogen acceptor on inosinate oxidation is NAD+. Finally, carbon 2 gains the amino group by spending an ATP molecule (which becomes AMP+2Pi).
Numerous organic compounds have other common names, often originating in historical source material thereof. The systematic IUPAC name is not always the preferred IUPAC name , for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid.
The structure of carbodicarbenes greatly resembles that of carbodiphosphoranes. [4] Computational data for a N-methyl-substituted carbodicarbene predicted a carbon-carbon bond with a length only marginally longer than a C=C bond in a typical allene at 1.358 Å (compared with 1.308 Å for allene), but with a significantly bent bond angle of 131.8° (compared to 180° for a standard linear ...
Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.
Carbon-based compounds form the basis of all known life on Earth, and the carbon-nitrogen-oxygen cycle provides a small portion of the energy produced by the Sun, and most of the energy in larger stars (e.g. Sirius). Although it forms an extraordinary variety of compounds, most forms of carbon are comparatively unreactive under normal conditions.