75209-54-0 Usage
Description
1-(3-methoxyphenyl)cycloheptene, with the molecular formula C14H18O, is a chemical compound that features a cycloheptene ring with a methoxyphenyl group attached to the first carbon atom. This cyclic hydrocarbon is a versatile building block in organic synthesis, allowing for the creation of various other compounds through different chemical reactions. It is also utilized in pharmaceutical research and development for the synthesis of potential drug candidates. As a colorless liquid with a faint odor, 1-(3-methoxyphenyl)cycloheptene should be handled with care due to its flammability at high temperatures and potential hazards if ingested, inhaled, or comes into contact with the skin.
Uses
Used in Organic Synthesis:
1-(3-methoxyphenyl)cycloheptene is used as a building block in organic synthesis for the creation of various compounds. Its unique structure allows for a wide range of chemical reactions, making it a valuable component in the development of new molecules with diverse applications.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 1-(3-methoxyphenyl)cycloheptene is used as a key component in the synthesis of potential drug candidates. Its versatility in chemical reactions enables the exploration of new therapeutic agents with the potential to address various medical conditions.
Used in Chemical Research:
1-(3-methoxyphenyl)cycloheptene is also utilized in chemical research to study the properties and reactivity of cycloheptene rings and methoxyphenyl groups. This knowledge can contribute to the advancement of synthetic chemistry and the development of novel compounds with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 75209-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,0 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75209-54:
(7*7)+(6*5)+(5*2)+(4*0)+(3*9)+(2*5)+(1*4)=130
130 % 10 = 0
So 75209-54-0 is a valid CAS Registry Number.
75209-54-0Relevant articles and documents
Pd-catalyzed cross-coupling of highly sterically congested enol carbamates with grignard reagents via c-o bond activation
Chen, Zicong,So, Chau Ming
, p. 3879 - 3883 (2020/06/08)
The palladium-catalyzed cross-coupling reaction of enol carbamates to construct highly sterically congested alkenyl compounds is presented for the first time. This protocol demonstrates the potential of using thermally stable and highly atom-economic enol electrophiles as building blocks in bulky alkene synthesis. This reaction accommodates a broad substrate scope with excellent Z/E isomer ratios, which also provides a new synthetic pathway for accessing Tamoxifen.
Well-defined air-stable palladium HASPO complexes for efficient Kumada-Corriu cross-couplings of (Hetero)aryl or alkenyl tosylates
Ackermann, Lutz,Kapdi, Anant R.,Fenner, Sabine,Kornhaab, Christoph,Schulzke, Carola
supporting information; experimental part, p. 2965 - 2971 (2011/05/05)
Palladium complexes of representative heteroatom-substituted secondary phosphine oxide (HASPO) preligands were synthesized and fully characterized, including X-ray crystal structure analysis. Importantly, these well-defined complexes served as highly efficient catalysts for Kumada-Corriu cross-coupling reactions of aryl, alkenyl, and even heteroaryl tosylates. Particularly, an air-stable catalyst derived from inexpensive PinP(O)H displayed a remarkably high catalytic efficacy, which resulted in cross-couplings at low catalyst loadings under exceedingly mild reaction conditions with ample scope.