83960-80-9

Basic information

• Product Name: 3-(2-Carboxy-5-methoxy-phenyl)-propionsaeure
• Synonyms: 3-(2-Carboxy-5-methoxy-phenyl)-propionsaeure
• CAS NO: 83960-80-9
• Molecular Weight: 224.213
• Mol File: 83960-80-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(2-Carboxy-5-methoxy-phenyl)-propionsaeure(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-Carboxy-5-methoxy-phenyl)-propionsaeure(83960-80-9)
• EPA Substance Registry System: 3-(2-Carboxy-5-methoxy-phenyl)-propionsaeure(83960-80-9)

Safety Data

• Hazardous Substances Data: 83960-80-9(Hazardous Substances Data)

Upstream product

• 70157-84-5 6-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl acetate 
• 16821-32-2 6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol 
• 16821-33-3 7-methoxy-3-(6'-methoxy-1',2',3',4',-tetrahydronaphth-1'-yl)-1,2-dihydronaphthalene 
• 67-64-1 acetone 
• 952006-66-5 5-methoxy-1-oxo-indan-2-carbaldehyde 
• 873422-55-0 5-methoxy-1-oxo-indan-2-carbonitrile 
• 52178-91-3 7-methoxy-1,2-dihydronaphthalene 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 69841-41-4 14α,17β-Diacetoxy-3-methoxy-8,14-secoestra-1,3,5(10),9(11)-tetraen 
• 132432-05-4 2-furfurylidene-6-methoxy-3,4-dihydronaphthalen-1(2H)-one 
• 83998-55-4 17β-Acetoxy-3-methoxy-8,14-secoestra-1,3,5(10),9(11)-tetraen-14-on 
• 25221-98-1 2-[(2E)-2-(6-methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)-ethyl]-2-methylcyclopentane-1,3-dione 

Downstream Products

• 82976-54-3 3-(2-Hydroxymethyl-5-methoxy-phenyl)-propan-1-ol 
• 5111-70-6 5-methoxy-1-indanone 
• 65272-96-0 3-(2-methyl-5-methoxyphenyl)propanol 
• 136035-99-9 4-Methoxy-2-(2-methoxycarbonyl-ethyl)-benzoic acid methyl ester 

Relevant articles and documents

Synthetic Investigations on Illudinine: A New Synthesis of Methyl 8-Methoxy-2,2-dimethyl-7-oxo-1,2,3,5,6,7-hexahydro-s-indacene-4-carboxylate

A new strategy for the total synthesis of methyl 8-methoxy-2,2-dimethyl-7-oxo-1,2,3,5,6,7,-hexahydro-s-indacene-4-carboxylate 4, a key intermediate in the synthesis of illudalanes, is reported.The key step in this strategy is a new method of preparation o

BORON ANNULATION: SYNTHESIS OF TRANS-DECALIN NATURAL PRODUCT SYNTHONS

Boron annulation of olefines 3, 4 and 14 has afforded decalin synthons 1 and 2 and perhydrophenanthrone 15, respectively.The A, B ring juncture of 15 and the ring systems of 1 and 2 were found to be trans.