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5353-15-1

5353-15-1 structure
5353-15-1 structure
  • Name: γ-Asarone
  • Chemical Name: 1,2,4-trimethoxy-5-prop-2-enylbenzene
  • CAS Number: 5353-15-1
  • Molecular Formula: C12H16O3
  • Molecular Weight: 208.25400
  • Catalog: Research Areas Inflammation/Immunology
  • Create Date: 2017-11-26 23:32:20
  • Modify Date: 2024-01-05 10:37:52
  • γ-Asarone, a phenylpropene, shows strong correlation with the biological activities (anti-oxidative, anti-inflammatory and neurotrophic effects)[1].
Name 1,2,4-trimethoxy-5-prop-2-enylbenzene
Synonyms (2,4,5-trimethoxyphenyl)prop-1-ene
1,2,4-TRIMETHOXY-5-ALLYLBENZENE
Benzene,1,2,4-trimethoxy-5-(2-propenyl)
2,4,5-Trimethoxyallylbenzene
1-Allyl-2,4,5-trimethoxy-benzol
1-allyl-2,4,5-trimethoxybenzene
Description γ-Asarone, a phenylpropene, shows strong correlation with the biological activities (anti-oxidative, anti-inflammatory and neurotrophic effects)[1].
Related Catalog
In Vitro γ-asarone epoxide is a terminal epoxide. γ-asarone epoxide was not mutagenic under any conditions[1].
References

[1]. Kerstin Berg, et al. Comparative investigation of the mutagenicity of propenylic and allylic asarone isomers in the Ames fluctuation assay. Mutagenesis. 2016 Jul;31(4):443-51.
Density 1.011g/cm3
Boiling Point 287.7ºC at 760 mmHg
Molecular Formula C12H16O3
Molecular Weight 208.25400
Flash Point 95.4ºC
Exact Mass 208.11000
PSA 27.69000
LogP 2.44090
Index of Refraction 1.496
HS Code 2909309090
135-77-3 structure

135-77-3

~89%

5353-15-1 structure

5353-15-1
Literature: Dieter, Janice W.; Li, Zhong; Nicholas, Kenneth M. Tetrahedron Letters, 1987 , vol. 28, # 45 p. 5415 - 5418
437761-99-4 structure

437761-99-4

~44%

5353-15-1 structure

5353-15-1
Literature: Sinha, Arun K.; Acharya, Ruchi; Joshi, Bhupendra P. Journal of Natural Products, 2002 , vol. 65, # 5 p. 764 - 765
490-64-2 structure

490-64-2
106-95-6 structure

106-95-6

~87%

5353-15-1 structure

5353-15-1
Literature: Wang, Jiantao; Cui, Zili; Zhang, Yuexia; Li, Huajie; Wu, Long-Min; Liu, Zhongquan Organic and Biomolecular Chemistry, 2011 , vol. 9, # 3 p. 663 - 666
67-56-1 structure

67-56-1
93-15-2 structure

93-15-2

~%

5353-15-1 structure

5353-15-1
Literature: Wang, Shaopeng; Swenton, John S. Tetrahedron Letters, 1990 , vol. 31, # 11 p. 1513 - 1516
5273-86-9 structure

5273-86-9

~%

5353-15-1 structure

5353-15-1
Literature: Sinha, Arun K.; Acharya, Ruchi; Joshi, Bhupendra P. Journal of Natural Products, 2002 , vol. 65, # 5 p. 764 - 765
99217-07-9 structure

99217-07-9

~%

5353-15-1 structure

5353-15-1
Literature: Sinha, Arun K.; Acharya, Ruchi; Joshi, Bhupendra P. Journal of Natural Products, 2002 , vol. 65, # 5 p. 764 - 765
2033-89-8 structure

2033-89-8
106-95-6 structure

106-95-6
77-78-1 structure

77-78-1

~%

5353-15-1 structure

5353-15-1

Detail
Literature: Greca, Marina Della; Monaco, Pietro; Pollio, Antonino; Previtera, Lucio Phytochemistry (Elsevier), 1992 , vol. 31, # 12 p. 4119 - 4124
6906-64-5 structure

6906-64-5
74-88-4 structure

74-88-4

~%

5353-15-1 structure

5353-15-1
Literature: Shulgrin,A.T. Canadian Journal of Chemistry, 1965 , vol. 43, p. 3437 - 3440
HS Code 2909309090
Summary 2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

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