188656-65-7 Usage
Molecular weight
285.37 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Indole-4-carboxylic acid, 3-[(phenylmethyl)thio]-, methyl ester The structure of the compound is a graphical representation of the arrangement of atoms in the molecule.
Derivation
Indole-4-carboxylic acid The compound is derived from indole-4-carboxylic acid, which is a naturally occurring organic compound.
Substituents
Methyl ester, phenylmethylthio The compound contains a methyl ester group and a phenylmethylthio substituent, which are functional groups that are attached to the indole ring.
Biological activity
Potential biological activities The compound may have potential biological activities, which are of interest for further research in the fields of drug discovery and development.
Use
Organic synthesis, medicinal chemistry The compound is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 188656-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,6,5 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188656-65:
(8*1)+(7*8)+(6*8)+(5*6)+(4*5)+(3*6)+(2*6)+(1*5)=197
197 % 10 = 7
So 188656-65-7 is a valid CAS Registry Number.
188656-65-7Relevant academic research and scientific papers
Connolly, Terrence J.,Durst, Tony
, p. 1337 - 1340 (1997)
A re-examination of a previously thought general synthesis of sultines from δ-hydroxy sulfoxides is shown to be more complicated than originally believed. The products obtained can be α,α'-dihaloxylenes or δ-halosulfones. The results are best interpreted based on carbocation stability of the key oxo-sulfoxonium salt intermediate.
