7469-81-0 Usage
Description
(1-bromocyclohexyl)(4-methoxyphenyl)methanone is a chemical compound derived from bromocyclohexane and 4-methoxybenzaldehyde, with a molecular formula of C14H17BrO2. It is a white to off-white solid at room temperature and is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive molecules. Its unique structure and reactivity make it a valuable compound for research and development in the pharmaceutical industry.
Uses
Used in Organic Synthesis:
(1-bromocyclohexyl)(4-methoxyphenyl)methanone is used as a building block for the synthesis of various pharmaceuticals and bioactive molecules due to its unique structure and reactivity.
Used in Medicinal Chemistry:
(1-bromocyclohexyl)(4-methoxyphenyl)methanone is used as a starting material for the development of new drugs and pharmaceuticals, as it possesses potential biological activity and has been studied for its pharmacological properties.
Used in Pharmaceutical Industry:
(1-bromocyclohexyl)(4-methoxyphenyl)methanone is used as a valuable compound for research and development in the pharmaceutical industry, contributing to the discovery and creation of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 7469-81-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7469-81:
(6*7)+(5*4)+(4*6)+(3*9)+(2*8)+(1*1)=130
130 % 10 = 0
So 7469-81-0 is a valid CAS Registry Number.
7469-81-0Relevant articles and documents
Novel intermediate and processes for its preparation and conversion into a pharmacologically-active agent
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, (2008/06/13)
Processes for the preparation of Venlafaxine (IX) via the novel epoxy-nitrile intermediate (I), which when subjected to hydrogenation forms compound (X), and may subsequently be reduced to yield the desired product (IX). The epoxy-nitrile intermediate (I) itself may be synthesised via various alternative reaction strategies, from a range of starting materials. E.g. 4-methoxy-benzaldehyde (VI), upon treatment with cyclohexyl magnesium bromide yields compound (V). This in turn may be oxidised to yield compound (III), which forms compound (II) on treatment with an (x-keto-halogenation agent. Cyanation of compound (II), then yields the desired epoxy nitrile intermediate (I), from which Venlafaxine (IX) may be synthesised.
