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92847-88-6

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92847-88-6 Usage

Description

Cyclopropyl(3,4-dimethoxyphenyl)methanone is a chemical compound with the molecular formula C11H12O3. It is a ketone that contains a cyclopropyl ring and two methoxy (CH3O-) groups attached to a phenyl ring. The presence of both the cyclopropyl and methoxy groups in its structure contributes to its unique reactivity and properties, making it a valuable building block in organic chemistry.

Uses

Used in Organic Synthesis:
Cyclopropyl(3,4-dimethoxyphenyl)methanone is used as a starting material for the preparation of various pharmaceuticals and chemicals. Its unique reactivity and properties make it a valuable building block in organic chemistry.
Used in Pharmaceutical Industry:
Cyclopropyl(3,4-dimethoxyphenyl)methanone is used as a key intermediate in the development of new drugs. Its potential applications in the field of medicinal chemistry make it an important compound for the synthesis of innovative pharmaceuticals.
Used in Medicinal Chemistry:
Cyclopropyl(3,4-dimethoxyphenyl)methanone is used as a versatile building block in the design and synthesis of novel drug candidates. Its unique structural features and reactivity enable the development of new therapeutic agents with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 92847-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92847-88:
(7*9)+(6*2)+(5*8)+(4*4)+(3*7)+(2*8)+(1*8)=176
176 % 10 = 6
So 92847-88-6 is a valid CAS Registry Number.

92847-88-6Relevant articles and documents

Hypervalent iodine mediated direct one pot transformation of aldehydes to ketones

Sagara, Prateep Singh,Chebolu, Rajesh,Bahuguna, Ashish,Ravikumar

, p. 15011 - 15013 (2014)

An environmentally benign, step economical synthesis of ketones directly from aldehydes has been developed using hypervalent iodine as an oxidant. The key features of this protocol are its mild conditions without the use of any heavy and toxic metals for the synthesis of a wide range of ketones. the Partner Organisations 2014.

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