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Carbon disulfide (also spelled as carbon disulphide) is an inorganic compound with the chemical formula CS 2 and structure S=C=S. It is also considered as the anhydride of thiocarbonic acid . [ 8 ] It is a colorless, flammable, neurotoxic liquid that is used as a building block in organic synthesis.
Structure and properties Index of refraction, n D: 1.6276 at 20 °C Abbe number? Dielectric constant, ε r: 2.641 ε 0 at 20 °C Bond strength? Bond length? Bond angle? Magnetic susceptibility? Surface tension [1] 35.3 dyn/cm at 0 °C 32.3 dyn/cm at 20 °C Viscosity [2] 0.495 mPa·s at –10 °C 0.436 mPa·s at 0 °C 0.380 mPa·s at 5 °C 0.363 ...
The prototype of a protein disulfide bond is the two-amino-acid peptide cystine, which is composed of two cysteine amino acids joined by a disulfide bond. The structure of a disulfide bond can be described by its χ ss dihedral angle between the C β −S γ −S γ −C β atoms, which is usually close to ±90°.
These fragments were then used as building blocks in the structure generator. This structure generator was part of a CASE system, ESESOC. [23] Breadth-first search generation. Molecular structure generation is explained step by step. Starting from a set of atoms, bonds are added between atom pairs until reaching saturated structures.
The bond angle for a symmetric tetrahedral molecule such as CH 4 may be calculated using the dot product of two vectors. As shown in the diagram at left, the molecule can be inscribed in a cube with the tetravalent atom (e.g. carbon) at the cube centre which is the origin of coordinates, O. The four monovalent atoms (e.g. hydrogens) are at four ...
Sulfides, formerly known as thioethers, are characterized by C−S−C bonds [3] [4] Relative to C−C bonds, C−S bonds are both longer, because sulfur atoms are larger than carbon atoms, and about 10% weaker. Representative bond lengths in sulfur compounds are 183 pm for the S−C single bond in methanethiol and 173 pm in thiophene.
Stereochemistry demands special attention because three-dimensionality is the most difficult part of a structure to visualize. Techniques for presenting 3-dimensional structures reflect the tastes of the artist. Three dimensionality is best highlighted by the depictions of bonds, using wedges, bolding, and hashed formats.
methyl groups attached to a ring or as branches in a longer carbon chain; methyl groups at the end of a carbon chain. If labels for structures are desired, consider the use of bolded numerals, which are language-neutral. Information about stereocenters and stereoisomerism should be included if available (e.g. by using wedged bonds).