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The chemical compound "(2S,6'R)-(7-chloro-4,6-dimethoxy-benzofuran-3-one)-2-spiro-1'-(2'-ethoxy-6'-methyl-cyclohex-2'-en-4'-one)" is a complex, chiral molecule with a unique structure. It features a benzofuran-3-one core, which is a type of aromatic heterocyclic compound, with a chlorine atom at the 7-position and two methoxy groups at the 4 and 6 positions. The molecule is further characterized by a spiro connection to a cyclohexenone ring, which is a six-membered carbon ring with a double bond and a ketone group. The cyclohexenone ring is substituted with an ethoxy group at the 2' position and a methyl group at the 6' position. The stereochemistry of the molecule is defined by the (2S,6'R) configuration, indicating the specific arrangement of atoms in three-dimensional space. (2S,6'R)-(7-chloro-4,6-dimethoxy-benzofuran-3-one)-2-spiro-1'-(2'-ethoxy-6'-methyl-cyclohex-2'-en-4'-one) is likely to have specific applications in the field of organic chemistry, potentially as a pharmaceutical intermediate or a precursor in the synthesis of other complex molecules.

3260-51-3

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3260-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3260-51-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3260-51:
(6*3)+(5*2)+(4*6)+(3*0)+(2*5)+(1*1)=63
63 % 10 = 3
So 3260-51-3 is a valid CAS Registry Number.

3260-51-3Downstream Products

3260-51-3Relevant academic research and scientific papers

Photodegradation of antimycotic drugs. 4. Communication: Photodegradation of flucytosine and griseofulvin

Thoma,Kuebler,Reimann

, p. 455 - 463 (2007/10/03)

The antimycotic drug substances flucytosine and griseofulvin are degraded under the influence of light. A liquid chromatography-mass spectrometry system helped us to elucidate some of the photodegradation pathways. 5-Fluorouracil is one of the photodegradation products of flucytosine in aqueous solution. The photodegradation of griseofulvin in solutions is mainly influenced by the solvent. The photodegradation product deschlorgriseofulvin could be detected in aqueous solution as well as in ethanolic and methanolic solution. Two photodegradation products found in ethanolic solution could, however, not be detected in methanolic or aqueous solution. Storage instructions of the pharmocopoeias are quite surprising. The US and the German pharmacopoeia recommend light protected storage for flucytosine but not for griseofulvin although griseofulvin is photodegraded more rapidly than flucytosine.

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