61936-95-6

Basic information

• Product Name: 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-1-(phenylmethyl)-, methyl ester
• CAS NO: 61936-95-6
• Molecular Formula: C18H17NO3
• Molecular Weight: 295.338
• Mol File: 61936-95-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-1-(phenylmethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-1-(phenylmethyl)-, methyl ester(61936-95-6)
• EPA Substance Registry System: 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-1-(phenylmethyl)-, methyl ester(61936-95-6)

Safety Data

• Hazardous Substances Data: 61936-95-6(Hazardous Substances Data)

Upstream product

• 125923-35-5 methyl (N¹-benzyl-3-indolyl)acetate 
• 100-39-0 benzyl bromide 
• 87-51-4 indole-3-acetic acid 
• 67-56-1 methanol 
• 85620-05-9 8-Benzyl-3a-hydroxy-3,3a,8,8a-tetrahydro-furo[2,3-b]indol-2-one 
• 85620-05-9 N-benzyl-2,3,3a,8aβ-tetrahydro-3aβ-hydroxyfuro(2,3-b)indol-2-one 
• 4307-97-5 N-benzylindole-3-acetic acid 

Downstream Products

• 1391913-56-6 C₃₄H₃₄N₂O₆ 
• 1391913-61-3 C₃₅H₃₆N₂O₆ 
• 1391913-62-4 C₃₅H₃₆N₂O₇ 
• 1391913-63-5 C₃₅H₃₃F₃N₂O₇ 
• 1391913-64-6 C₃₄H₃₃FN₂O₆ 
• 1391913-65-7 C₃₄H₃₃ClN₂O₆ 
• 1391913-66-8 C₃₄H₃₃BrN₂O₆ 
• 1391913-67-9 C₃₄H₃₃N₃O₈ 
• 1391913-68-0 C₃₄H₃₃ClN₂O₆ 
• 1391913-69-1 C₃₄H₃₃BrN₂O₆ 
• 1391913-70-4 C₃₄H₃₃ClN₂O₆ 
• 1391913-49-7 C₁₇H₁₇NO₂ 
• 1391913-52-2 C₁₇H₁₆BrNO 

Relevant articles and documents

An organocatalytic cascade strategy for the enantioselective construction of spirocyclopentane bioxindoles containing three contiguous stereocenters and two spiro quaternary centers

A rapid and efficient organocatalytic cascade sequence for the direct construction of spirocyclopentane bioxindoles has been carried out by using a chiral squaramide catalyst in the presence of a base. This process constitutes a powerful approach to the preparation of biologically important bispirooxindoles in high enantioselectivities (see scheme). Copyright

PHOTO-OXYGENATION OF INDOLE-3-ACETIC ACIDS AND INDOLE-3-ACETALDEHYDES: BIOMIMETIC CONVERSION OF INDOLES INTO QUINOLINES VIA N1-C2 FISSION

New conversion of indoles to quinolines via the N1-C2 fission using singlet oxygen reaction was investigated starting from indole-3-acetic acids and indole-3-acetaldehydes.Dye-induced photo-oxydation of indole-3-acetaldehyde derivatives (17 and 18) followed by treatments with dimethyl sulfide and then acetic acid produced 4-formyl- and 4-acetylquinolines (19 and 20), respectively.