62558-13-8 Usage
Main Properties
1. Molecular Formula: C27H36O6S
2. Functional Groups:
Sulfanyl group (-S)
Carboxylic acid group (-COOH)
Hydroxypropan-2-yl groups (-CH2CH(OH)CH3)
3. Substituents on Benzene Ring:
Tert-butyl group (-C(CH3)3)
Hydroxypropan-2-yl group (-CH2CH(OH)CH3)
Specific Content
1. Sulfanyl Group:
Contains a sulfur atom bonded to an alkyl or aryl group.
Provides chemical reactivity and potential for forming coordination complexes.
2. Carboxylic Acid Group:
Contains a carboxyl group (-COOH) that can act as an acid.
Contributes to the compound's acidity and ability to form salts.
3. Hydroxypropan-2-yl Groups:
Hydroxypropan-2-yl groups are attached to both the benzene ring and the carboxylic acid group.
Can participate in hydrogen bonding and influence the compound's solubility and interactions.
4. Benzene Ring with Substituents:
Contains a benzene ring with tert-butyl and hydroxypropan-2-yl substituents.
Substituents can affect the compound's steric hindrance, stability, and chemical properties.
5. Potential Applications:
Due to its diverse functional groups and structural complexity, the compound may have applications in pharmaceuticals, agrochemicals, or materials.
Specific uses could include drug development, pesticide formulations, or as a component in advanced materials.
6. Research Needs:
Further research is necessary to fully understand the compound's properties, potential reactivity, and applications.
Detailed studies are needed to explore its biological activity, environmental impact, and synthetic pathways for industrial purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 62558-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62558-13:
(7*6)+(6*2)+(5*5)+(4*5)+(3*8)+(2*1)+(1*3)=128
128 % 10 = 8
So 62558-13-8 is a valid CAS Registry Number.
62558-13-8Relevant academic research and scientific papers
Apical Ligand Preference and Fluxional Behavior of Some Sulfuranes
Lam, William Y.,Martin, J. C.
, p. 4468 - 4473 (2007/10/02)
Sulfides 4, 11, and 12 react with m-chloroperbenzoic acid to form apically unsymmetrically substituted sulfuranes 18-20, respectively, instead of the isomeric symmetrically substituted dialkoxysulfuranes.Rapid equilibration (ΔG*12 deg C = 14.7 kcal mol-1) of isomers of sulfurane 18 is observed and studied by (1)H NMR spectroscopy.An associative mechanism for these interconversion processes is proposed.Potassium salts of 18 and 19 are symmetrical dialkoxysulfuranes 21 and 22, respectively.Other reactions involving these sulfuranes are also reported.
Diaryltetraoxypersulfuranes: Preparation, Characterization, and Reactions
Lam, William Y.,Martin, J. C.
, p. 120 - 127 (2007/10/02)
Diarylbis(acyloxy)dialkyloxypersulfurane 7, the first example of hexacoordinate organosulfur(VI) derivative lacking fluorine ligands, a sulfone bisketal, was synthesized by treatment of sulphide diol diacid 6 with pyridine and tert-butyl hypochlorite at 0
