58621-52-6 Usage
Carbonyl group attachment
Attached to the sixth carbon atom of the 1-ChroMan ring This describes the specific location of the carbonyl group within the compound's structure.
Use as a reagent
Organic synthesis and pharmaceutical research 1-ChroMan-6-yl-ethanone is often used as a reagent, which means it is a substance that aids or accelerates a chemical reaction in these fields.
Unique structure
The compound's specific arrangement of atoms This refers to the distinct pattern of bonds and atoms in the 1-ChroMan-6-yl-ethanone molecule.
Potential reactivity
Possesses possible reactive properties This indicates that the compound may readily undergo chemical reactions or transformations.
Pharmacological properties
Studied for its potential effects on living organisms This means that researchers are investigating the compound's possible impact on biological systems and potential therapeutic uses.
Biological activities
Investigated for its interactions with biological systems This refers to the compound's possible effects on biological processes or organisms.
Applications in drug development
May have applications in the development of new drugs or therapeutic agents This suggests that 1-ChroMan-6-yl-ethanone could potentially be used as a basis for creating new medications or treatments.
Versatile chemical
Holds promise for various scientific and industrial applications This highlights the compound's potential for use in a wide range of fields and industries.
Check Digit Verification of cas no
The CAS Registry Mumber 58621-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58621-52:
(7*5)+(6*8)+(5*6)+(4*2)+(3*1)+(2*5)+(1*2)=136
136 % 10 = 6
So 58621-52-6 is a valid CAS Registry Number.
58621-52-6Relevant articles and documents
Lewis Acid Catalyzed Transfer Hydromethallylation for the Construction of Quaternary Carbon Centers
Walker, Johannes C. L.,Oestreich, Martin
, p. 15386 - 15389 (2019/10/28)
The design and gram-scale synthesis of a cyclohexa-1,4-diene-based surrogate of isobutene gas is reported. Using the highly electron-deficient Lewis acid B(C6F5)3, application of this surrogate in the hydromethallylation of electron-rich styrene derivatives provided sterically congested quaternary carbon centers. The reaction proceeds by C(sp3)?C(sp3) bond formation at a tertiary carbenium ion that is generated by alkene protonation. The possibility of two concurrent mechanisms is proposed on the basis of mechanistic experiments using a deuterated surrogate.
DERIVATIVES OF BENZOTHIAZINES, PREPARATION THEREOF AND APPLICATION THEREOF AS DRUGS
-
, (2010/09/18)
The object of the present invention is benzothiazine derivatives having the capability of inhibiting 11β-HSD1 not only at an enzymatic level but also at a cell level. The compounds of the present invention are of general formula (I). Wherein notably R1 represents a hydrogen or OR1 represents an ester or an ether. R2 represents a naphthyl or a 1, 2, 3, 4-tetrahydro-naphthalene or a biphenyl or phenyl pyridine or a substituted phenyl. R3 represents a methyl or ethyl; R4 and R'4 represent a hydrogen.
TRICYCLIC 1,2,4-TRIAZINE OXIDES AND COMPOSITIONS THEREFROM FOR THERAPEUTIC USE IN CANCER TREATMENTS
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, (2008/06/13)
The invention relates to novel tricyclic 1,2,4-triazine-1-oxides and novel tricyclic 1,2,4-triazine-1,4-dioxides of formula: (I); and to related analogues, to their preparation, and to their use as hypoxia-selective drugs and radiosensitizers for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.
