93170-65-1 Usage
Chemical Class
Benzoates
Explanation
1,4-Benzodithiin-6-ol, 2,3-dihydro-, benzoate belongs to the class of benzoates, which are derivatives of benzoic acid.
Explanation
The compound consists of a benzene ring fused to a dithiin ring, which is a seven-membered ring containing two sulfur atoms.
Explanation
The molecule contains a hydroxyl (-OH) group attached to the 6th carbon of the dithiin ring and a benzoate ester group, which is derived from benzoic acid.
Explanation
Due to its unique structure and properties, 1,4-Benzodithiin-6-ol, 2,3-dihydro-, benzoate may have applications in the development of pharmaceuticals and agrochemicals.
Explanation
The compound can act as a ligand in organic synthesis and coordination chemistry, which involves the formation of complexes with metal ions.
Explanation
1,4-Benzodithiin-6-ol, 2,3-dihydro-, benzoate can be used as a building block for the synthesis of new materials and compounds for various industrial and research purposes.
Explanation
As a derivative of benzoic acid with a hydroxyl group, the compound is expected to be soluble in organic solvents such as ethanol, methanol, and acetone.
Explanation
The compound is likely stable under normal conditions, such as room temperature and pressure, due to its aromatic nature and the presence of the benzoate ester.
Explanation
The presence of the hydroxyl group and the benzoate ester in the molecule suggests that 1,4-Benzodithiin-6-ol, 2,3-dihydro-, benzoate may undergo reactions with nucleophiles (such as amines and thiols) and electrophiles (such as halogens and strong acids).
Explanation
The toxicity of 1,4-Benzodithiin-6-ol, 2,3-dihydro-, benzoate is not explicitly mentioned, but due to its chemical structure and potential applications in pharmaceuticals and agrochemicals, it may have moderate to high toxicity. Further studies would be required to determine its exact toxicity profile.
Structure
Combination of benzene and dithiin rings
Functional Groups
Hydroxyl group and benzoate ester
Potential Applications
Pharmaceuticals and agrochemicals
Role as a Ligand
Organic synthesis and coordination chemistry
Building Block
Creation of new materials and compounds
Solubility
Likely soluble in organic solvents
Stability
Stable under normal conditions
Reactivity
May react with nucleophiles and electrophiles
Toxicity
Unknown, but potential for moderate to high toxicity
Check Digit Verification of cas no
The CAS Registry Mumber 93170-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,7 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93170-65:
(7*9)+(6*3)+(5*1)+(4*7)+(3*0)+(2*6)+(1*5)=131
131 % 10 = 1
So 93170-65-1 is a valid CAS Registry Number.
93170-65-1Relevant academic research and scientific papers
A ROUTE TO FUNCTIONALISED CYCLOPENTANES FROM 6-DEOXYHEX-5-ENOPYRANOSIDE DERIVATIVES
Ferrier, Robert J.,Haines, Stephen R.
, p. 135 - 146 (2007/10/02)
A route to the functionalised cyclopentenone derivative, (2S)-(2/3)-dibenzyloxy-5-(hydroxymethyl)cyclopentene-4-enone ethylene acetal, has been developed from a deoxyinosose that is readily accessible.The carbocyclisation procedure was less efficient in a
