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Chemical Structure| 4407-36-7 Chemical Structure| 4407-36-7
Chemical Structure| 4407-36-7

trans-Cinnamyl alcohol

CAS No.: 4407-36-7

trans-Cinnamyl alcohol is the trans-isomer of cinnamyl alcohol and an active compound isolated from chestnut flowers. It has anti-obesity effects by modulating adipocyte function and fat accumulation through the inhibition of increased PPARγ expression.

Synonyms: trans-Cinnamyl alcohol

4.5 *For Research Use Only !

Cat. No.: A194226 Purity: 97%

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Product Citations

Product Citations

Kumar, Vikas ; Johnson, Bryce P. ; Dimas, Dustin A. ; Singh, Shanteri ;

Abstract: The widespread utility of isoprenoids has recently sparked interest in efficient synthesis of isoprene-diphosphate precursors. Current efforts have focused on evaluating two-step "isoprenol pathways," which phosphorylate prenyl alcs. using promiscuous kinases/phosphatases. The convergence on isopentenyl phosphate kinases (IPKs) in these schemes has prompted further speculation about the class's utility in synthesizing non-natural isoprenoids. However, the substrate promiscuity of IPKs in general has been largely unexplored. Towards this goal, authors report the biochem. characterization of five novel IPKs from Archaea and the assessment of their substrate specificity using 58 alkyl-monophosphates. This study reveals the IPK-catalyzed synthesis of 38 alkyl-diphosphate analogs and discloses broad substrate specificity of IPKs. Further, to demonstrate the biocatalytic utility of IPK-generated alkyl-diphosphates, they also highlight the synthesis of alkyl-L-tryptophan derivatives using coupled IPK-prenyltransferase reactions. These results reveal IPK-catalyzed reactions are compatible with downstream isoprenoid enzymes and further support their development as biocatalytic tools for the synthesis of non-natural isoprenoids.

Keywords: alternate mevalonate pathway ; biocatalysis ; enzyme promiscuity ; natural products ; terpenoid

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Product Details of trans-Cinnamyl alcohol

CAS No. :4407-36-7
Formula : C9H10O
M.W : 134.18
SMILES Code : OC/C=C/C1=CC=CC=C1
Synonyms :
trans-Cinnamyl alcohol
MDL No. :MFCD00002921
InChI Key :OOCCDEMITAIZTP-QPJJXVBHSA-N
Pubchem ID :5315892

Safety of trans-Cinnamyl alcohol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H317-H319
Precautionary Statements:P261-P264-P270-P272-P280-P301+P312+P330-P302+P352+P333+P313+P363-P305+P351+P338+P337+P313-P501

Application In Synthesis of trans-Cinnamyl alcohol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4407-36-7 ]

[ 4407-36-7 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 1986-47-6 ]
  • [ 21087-29-6 ]
  • [ 4407-36-7 ]
  • 2
  • [ 6638-05-7 ]
  • [ 4407-36-7 ]
  • (1S*,3R*,6R*,7R*,10R*)-1,3-dimethoxy-8-methyl-10-phenyl-4-oxatricyclo<4.3.1.03,7>dec-8-en-2-one [ No CAS ]
  • 3
  • [ 3240-34-4 ]
  • [ 2896-67-5 ]
  • [ 4407-36-7 ]
  • [ 611-68-7 ]
  • 4-hydroxy-3-methoxy-5-methylphenyl acetate [ No CAS ]
  • (+/-)-(1R,3R,6S,7R,10S)-3-methoxy-1-methyl-10-phenyl-4-oxatricyclo[4.3.1.03,7]dec-8-en-2-one [ No CAS ]
  • (+/-)-(1R,3R,6R,7S,10R)-3-methoxy-1-methyl-2-oxo-10-phenyl-4-oxatricyclo[4.3.1.03,7]dec-8-en-8-yl acetate [ No CAS ]
  • 4
  • [ 120870-47-5 ]
  • [ 4407-36-7 ]
  • [ 1357469-14-7 ]
  • 5
  • [ 2439-54-5 ]
  • [ 4407-36-7 ]
  • [ 1415608-51-3 ]
  • 6
  • [ 4407-36-7 ]
  • [ 23020-15-7 ]
  • 7
  • [ 4407-36-7 ]
  • [ 185256-47-7 ]
  • 8
  • [ 20026-96-4 ]
  • [ 4407-36-7 ]
  • ethyl (2R,3R)-2-(4-chlorobenzoyl)-3-phenylpent-4-enoate [ No CAS ]
  • ethyl 2-(4-chlorobenzoyl)-3-phenylpent-4-enoate [ No CAS ]
  • 9
  • [ 20026-96-4 ]
  • [ 4407-36-7 ]
  • ethyl 2-(4-chlorobenzoyl)-3-phenylpent-4-enoate [ No CAS ]
  • 10
  • [ 107-75-5 ]
  • [ 4407-36-7 ]
  • (1E)-10-hydroxy-6,10-dimethyl-1-phenyl-1-undecen-4-one [ No CAS ]
 

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