32910-58-0 Usage
Description
4-(heptylsulfanyl)benzoic acid is an organic chemical compound characterized by the molecular formula C14H20O2S. It features a benzene ring with a carboxylic acid group and a heptylthio (C7H15S) group attached to it. 4-(heptylsulfanyl)benzoic acid is known for its unique properties due to the heptylthio group, which makes it valuable in various industrial and research applications, as well as in the synthesis of other organic compounds.
Uses
Used in Pharmaceutical Production:
4-(heptylsulfanyl)benzoic acid is used as a key intermediate in the synthesis of pharmaceuticals for its unique chemical properties that can be leveraged to create new drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(heptylsulfanyl)benzoic acid is utilized as a component in the development of various agrochemicals, potentially enhancing the effectiveness of these products in agricultural applications.
Used in Dye Manufacturing:
4-(heptylsulfanyl)benzoic acid is also employed in the production of dyes, where its chemical structure contributes to the color and stability of the dyes produced.
Used as an Intermediate in Organic Synthesis:
4-(heptylsulfanyl)benzoic acid serves as an intermediate in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical products across different industries.
Given the potential biological and physiological effects of 4-(heptylsulfanyl)benzoic acid, further research may uncover additional applications in various fields, including but not limited to medicine, agriculture, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 32910-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,1 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32910-58:
(7*3)+(6*2)+(5*9)+(4*1)+(3*0)+(2*5)+(1*8)=100
100 % 10 = 0
So 32910-58-0 is a valid CAS Registry Number.
32910-58-0Relevant articles and documents
Hydrogen bonding liquid crystalline benzoic acids with alkylthio groups: Phase transition behavior and insights into the cybotactic nematic phase
Arakawa, Yuki,Sasaki, Yukito,Igawa, Kazunobu,Tsuji, Hideto
, p. 6514 - 6522 (2017/07/17)
A simple but novel class of hydrogen bonding liquid crystalline benzoic acids with alkylthio (or alkylsulfanyl; SR) groups was established. In general, although it is difficult for laterally non-substituted rod-like molecules with an alkylthio group to form some mesophases, the present molecules exclusively form a nematic (N) regime, owing to spontaneous carboxylic dimerization. It was found that the number of carbons in the alkylthio groups strongly correlated with transition temperatures as well as nematogenic stability: odd-even effects. Even-members displayed wider monotropic and enantiotropic N phases, despite the fact that almost all odd-members showed either none or only monotropic-narrower ones. Interestingly, their thermal transition temperatures were lower compared to those for alkoxy (OR) analogues, on account of the small angle (or large bend) of the C-S-C bond as well as the low electron density on their aromatic ring due to the weak electron donor properties of alkylthio groups. Additionally, in-depth wide-angle X-ray diffraction measurements revealed that an alkylthio analogue exhibited significantly enhanced smectic clusters formed in the N regime (or Ncyb phase) as well as the cluster type close to smectic (Sm) A, in comparison with an alkoxy analogue exhibiting a clear SmC-type cluster. The results indicate that a robust S?S intermolecular interaction for an alkylthio group into a mesogen affects the kind of smectic cluster in the Ncyb phase.
