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Benzenemethanol, 4-bromo-α-(1-methylethenyl)-, also known as 4-bromo-α-(1-methylvinyl)benzyl alcohol or 4-bromo-α-methylstyrene-α-ol, is an organic compound with the chemical formula C9H11BrO. It is a derivative of benzyl alcohol, featuring a bromine atom at the 4-position and a 1-methylvinyl group attached to the α-carbon. Benzenemethanol, 4-bromo-a-(1-methylethenyl)- is characterized by its aromatic ring structure, which includes a hydroxyl group and a bromine atom, and a vinyl group attached to the side chain. It is used in various chemical reactions and synthesis processes, particularly in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits specific reactivity and properties that make it valuable in organic synthesis and as a building block for more complex molecules.

23596-90-9

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23596-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23596-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,9 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23596-90:
(7*2)+(6*3)+(5*5)+(4*9)+(3*6)+(2*9)+(1*0)=129
129 % 10 = 9
So 23596-90-9 is a valid CAS Registry Number.

23596-90-9Relevant academic research and scientific papers

Iron(III) Chloride/Phenylsilane-Mediated Cascade Reaction of Allyl Alcohols with Maleimides: Synthesis of Poly-Substituted γ-Butyrolactones

Zhang, Hua,Zhan, Xiao-Yu,Chen, Xu-Ling,Tang, Lei,He, Shuai,Shi, Zhi-Chuan,Wang, Yu,Wang, Ji-Yu

, p. 4919 - 4925 (2019)

A iron-catalyzed free radical cascade reaction of allyl alcohols with N-substituted maleimides for accessing poly-substituted γ-butyrolactones has been developed. In this protocol, various allyl alcohols can open N-substituted maleimide rings to form allyl ester intermediates, and the allyl ester intermediates can be converted into an allyl ester alkyl radicals and undergo intramolecular free radical addition cyclization to form a polysubstituted γ-butyrolactones. In this protocol, spiro γ-butyrolactone compounds can be also synthesized. Meanwhile, the strategy could be applied to further construct a fully substituted tetrahydrofuran. The reaction is not sensitive to oxygen or moisture and has been performed on gram-scale. (Figure presented.).

CATHEPSIN CYSTEINE PROTEASE INHIBITORS

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Page 64, (2010/02/06)

This invention relates to class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis. They have the following structure: Formula (I).

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