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3,3-dimethyl-3,4-dihydro-1H-benzo[c]chromene-1,6(2H)-dione is a complex organic compound with the molecular formula C13H12O3. It is a derivative of benzo[c]chromene, a type of aromatic compound with a benzene ring fused to a chromene ring. The structure features two methyl groups attached to the third carbon of the chromene ring, and a dihydro functional group, which indicates the presence of a hydrogenated double bond. The compound also contains two carbonyl groups, one at the first position and the other at the sixth position, with the latter being part of a 2H-diketone group. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and natural products, particularly those with antioxidant and anti-inflammatory properties. Its unique structure and functional groups make it an interesting target for further chemical and biological studies.

6315-06-6

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6315-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6315-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6315-06:
(6*6)+(5*3)+(4*1)+(3*5)+(2*0)+(1*6)=76
76 % 10 = 6
So 6315-06-6 is a valid CAS Registry Number.

6315-06-6Downstream Products

6315-06-6Relevant academic research and scientific papers

Rh(III)-catalyzed C-H activation of primary benzamides and tandem cyclization with cyclic 2-diazo-1,3-diketones for the synthesis of isocoumarins

He, Xinwei,Han, Guang,Zuo, Youpeng,Shang, Yongjia

, p. 7082 - 7088 (2018/10/24)

A simple and efficient Rh(III)-catalyzed C-H activation and tandem intramolecular cyclization for the synthesis of isocoumarins has been developed. The protocol uses easily available primary benzamides and cyclic 2-diazo-1,3-diketones as starting materials. This reaction proceeds via C-C and C-O bond formation in a single reaction vessel, and the corresponding isocoumarins were obtained in moderate to excellent yields (58%–97%). The well established protocol showed high functional group tolerance, which provided an efficient and alternative route to isocoumarin backbone.

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