118602-97-4

Basic information

• Product Name: Butanoic acid, 4-(phenylmethoxy)-, ethyl ester
• CAS NO: 118602-97-4
• Molecular Formula: C13H18O3
• Molecular Weight: 222.284
• Mol File: 118602-97-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Butanoic acid, 4-(phenylmethoxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 4-(phenylmethoxy)-, ethyl ester(118602-97-4)
• EPA Substance Registry System: Butanoic acid, 4-(phenylmethoxy)-, ethyl ester(118602-97-4)

Safety Data

• Hazardous Substances Data: 118602-97-4(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 4541-14-4 4-benzyloxy-butan-1-ol 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 26420-79-1 1-chloro-3-benzyloxypropane 
• 4799-68-2 3-benzyloxypropan-1-ol 
• 17229-17-3 benzyl 2-chloroethyl ether 
• 19340-86-4 N-benzyl-4-(benzyloxy)butanamide 
• 41478-45-9 Diethyl<(2-benzyloxy)ethyl>malonate 
• 85174-51-2 4-(benzyloxy)butyronitrile 

Downstream Products

• 1187663-04-2 C₁₉H₃₂O₄ 
• 1187663-05-3 diethyl 5-[3-(benzyloxy)propyl]nonanedioate 
• 1356140-46-9 10-[3-(benzyloxy)propyl]-2,18-dimethyl-6,14-bis(4-methylpentyl)nonadecane-6,14-diol 
• 1356140-27-6 6-[3-(benzyloxy)propyl]-2,10-dimethylundecan-6-ol 
• 1256492-93-9 (1,1-dimethylethyl)(dimethyl)({4-[(phenylmethyl)oxy]butyl}oxy)silane-d2 
• 31600-62-1 [1,1-2H₂]-4-benzyloxy-butan-1-ol 
• 1356140-45-8 10-[3-(benzyloxy)propyl]-2,18-dimethyl-6,14-bis(4-methylpentyl)nonadecan-10-ol 
• 1356140-32-3 1,9-bis(4-methoxybenzyloxy)-5-[3-(benzyloxy)propyl]nonan-5-ol 
• 1187663-07-5 C₃₅H₆₄O₂ 
• 1187663-06-4 C₁₉H₃₂O₂ 
• 856061-94-4 bis-(4-benzyloxy-butyl)-sulfide 
• 50873-93-3 [(4-chlorobutoxy)methyl]benzene 
• 130185-02-3 (+)-methyl 4-benzyloxy-2-(hydroxymethyl)butanoate 
• 143444-48-8 (S)-4-Benzyloxy-2-hydroxymethyl-butyric acid 

Relevant articles and documents

COMPOUND WITH BRANCHING ALKYL CHAINS, METHOD FOR PREPARING THE SAME, AND USE THEREOF IN PHOTOELECTRIC DEVICE

The invention discloses a compound having branching alkyl chains, the method for preparing the same and use thereof in photoelectric devices. By applying the branching alkyl chains as the solubilizing group to the preparation of organic conjugated molecules (for example, organic conjugated polymers), the number of methylenes between the resultant alky side chains and the backbone, i.e., m>1, which can effectively reduce the effect of the alkyl chains on the backbone π-π stacking, thereby ensuring the solubility of the organic conjugated molecule while greatly increasing the mobility of their carriers. It is suitable for an organic semiconductor material in photoelectric devices such as organic solar cells, organic light emitting diodes and organic field effect transistors, etc.

A new mild method for the cleavage of the amide bond: Conversion of secondary and tertiary amides to esters

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