7588-36-5

7588-36-5 structure

Name: Methyl 5-Methoxy-2-methylindole-3-acetate
Chemical Name: methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetate
CAS Number: 7588-36-5
Molecular Formula: C₁₃H₁₅NO₃
Molecular Weight: 233.26300
Create Date: 2018-12-25 16:53:12
Modify Date: 2025-08-27 11:57:45

Name	methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetate
Synonyms	Indole-3-acetic acid,5-methoxy-2-methyl-,methyl ester methyl 5-methoxy-2-methylindole-3-acetate methyl (5-methoxy-2-methyl-1H-indol-3-yl)acetate methyl [5-methoxy-2-methyl-indol-3-yl]-acetate 5-methoxy-2-methyl-1H-indole-3-acetic acid methyl ester 5-methoxy-2-methylindole-3-acetic acid methyl ester Methyl 5-methoxy-2-methyl-1H-indole-3-acetate (5-methoxy-2-methyl-1H-indol-3-yl)acetic acid methyl ester methyl-5-methoxy-2-methyl-3-indolylacetate

Molecular Formula	C₁₃H₁₅NO₃
Molecular Weight	233.26300
Exact Mass	233.10500
PSA	51.32000
LogP	2.20040

Hazard Codes	Xi

67-56-1

2882-15-7

~97%

7588-36-5

Literature: Liedtke, Andy J.; Marnett, Lawrence J.; Kim, Kwangho; Stec, Donald F.; Sulikowski, Gary A. Tetrahedron, 2012 , vol. 68, # 48 p. 10049 - 10058,10 Title/Abstract Show Details Liedtke, Andy J.; Kim, Kwangho; Stec, Donald F.; Sulikowski, Gary A.; Marnett, Lawrence J. Tetrahedron, 2012 , vol. 68, # 48 p. 10049 - 10058

2882-15-7

7588-36-5

Literature: Eli Lilly and Company Patent: US5578634 A1, 1996 ; US 5578634 A

624-45-3

19501-58-7

7588-36-5

Literature: Bitonti; Alan J.; McDonald; Ian A.; Salituro; Francesco G.; Whitten; Jeffrey P.; Jarvi; Esa T.; Wright; Paul S. Patent: US5877202 A1, 1999 ;

2882-15-7

75-36-5

~92%

7588-36-5

Literature: Chowdhury, Morshed A.; Huang, Zhangjian; Abdellatif, Khaled R.A.; Dong, Ying; Yu, Gang; Velazquez, Carlos A.; Knaus, Edward E. Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 19 p. 5776 - 5780

1076-74-0

96-34-4

7588-36-5

Literature: Gallant, Michel; Dufresne, Claude; Gareau, Yves; Guay, Daniel; Leblanc, Yves; Prasit, Petpiboon; Rochette, Chantal; Sawyer, Nicole; Slipetz, Deborah M.; Tremblay, Nathalie; Metters, Kathleen M.; Labelle, Marc Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 19 p. 2263 - 2268

53258-38-1

~84%

7588-36-5

Literature: Baccolini, Grazieno; Dalpozzo, Renato; Todesco, Paolo E. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988 , p. 971 - 974

53-86-1

7588-36-5

Literature: Scholz, Matthias; Blobaum, Anna L.; Marnett, Lawrence J.; Hey-Hawkins, Evamarie Bioorganic and Medicinal Chemistry, 2012 , vol. 20, # 15 p. 4830 - 4837

Precursor 8
67-56-1 2882-15-7 624-45-3 19501-58-7
75-36-5 53-86-1 1076-74-0 96-34-4
DownStream 6
1601-19-0 3285-40-3 1601-18-9 16401-76-6
1568-31-6 64160-54-9

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