6215-42-5 Usage
Naphthalene group
A two-ring aromatic system consisting of two fused benzene rings.
Benzothiophene group
A bicyclic aromatic system with one benzene ring and one thiophene ring.
Carboxylate ester
A functional group consisting of a carbonyl group (C=O) and an oxygen atom bonded to a carbon atom, which is present in the compound.
Amino group
A functional group consisting of a nitrogen atom bonded to two hydrogen atoms (-NH2), which is present in the compound.
Oxoethyl group
A functional group consisting of a carbonyl group (C=O) and an ethyl group (-CH2CH3), which is present in the compound.
Aromatic rings
The presence of the naphthalene and benzothiophene groups in the compound, which may contribute to its biological activity and physical properties.
Functional groups
The presence of the amino, carboxylate, and oxoethyl groups in the compound, which can participate in various chemical reactions and may have potential applications in organic synthesis, drug development, and material science.
Biological activity
The presence of the amino and carboxylate groups in the compound, which may contribute to its biological activity.
Physical properties
The presence of the conjugated aromatic systems in the compound, which may contribute to its physical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6215-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6215-42:
(6*6)+(5*2)+(4*1)+(3*5)+(2*4)+(1*2)=75
75 % 10 = 5
So 6215-42-5 is a valid CAS Registry Number.
6215-42-5Relevant academic research and scientific papers
Epoxidation versus Oxidation of Steroidal γ-Hydroxy-αβ-Unsaturated Ketones in Vanadium-catalyzed Reactions
Glotter, Erwin,Mendelovici, Marioara
, p. 2201 - 2235 (2007/10/02)
In the presence of t-butyl hydroperoxide and a catalytic amount of bis-acetylacetonato-oxovanadium, steroidal αβ-unsaturated ketones possessing an allylic hydroxy group behave in the same manner as simple allylic alcohols in cyclic systems without conformational flexibility.Equatorial OH groups give mainly oxidation products (2-ene-1, 4-diones), in most instances accompanied by cis and trans 2,3-epoxy-4-hydroxy-1-ones in a ratio of ca. 3:1.Axial OH groups give cis 2,3-epoxy-4-hydroxy-1-ones accompanied by small amounts of the corresponding 2-ene-1,4-diones.In two instances, reactants with an axial hydroxy group afforded mainly products resulting from oxidation of this group instead of epoxidation of the double bond.The exceptions are withanolide D (5β,6β-epoxy-4β,20-dihydroxy-1-oxowitha-2,24-dienolide) and 4α,5β-dihydroxycholest-2-ene-1-one.
