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(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95%

(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95% ??? ???
?? ??:
1940176-39-5
???:
(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95%
???(??):
(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone;Methanone, [4-(hydroxymethyl)phenyl][4-(2-propyn-1-yloxy)phenyl]-;(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95%
CBNumber:
CB73384487
???:
C17H14O3
??? ??:
266.29
MOL ??:
1940176-39-5.mol

(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95% ??

?? ?
461.4±45.0 °C(Predicted)
??
1.198±0.06 g/cm3(Predicted)
?? ??
-20°C
?? ?? (pKa)
13.90±0.10(Predicted)
??? ??
?? ?? ??

??

(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95% C??? ??, ??, ??

??

(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone is used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, alkyne tag, and hydroxyl synthetic handle. When appended to a ligand or pharmacophore through its hydroxyl linker, this building block allows for UV light-induced covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.

(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95% ?? ?? ? ???

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(4-(Hydroxymethyl)phenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone >=95% ?? ??

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