71616-83-6

Basic information

• Product Name: methyl 4-butyrylbenzoate
• Synonyms: methyl 4-butyrylbenzoate;4-butyrylbenzoic acid methyl ester
• CAS NO: 71616-83-6
• Molecular Formula: C₁₂H₁₄O₃
• Molecular Weight: 206.23776
• Mol File: 71616-83-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: 84 °C
• Boiling Point: 324.6±25.0 °C(Predicted)
• Appearance: /
• Density: 1.074±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: methyl 4-butyrylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-butyrylbenzoate(71616-83-6)
• EPA Substance Registry System: methyl 4-butyrylbenzoate(71616-83-6)

Safety Data

• Hazardous Substances Data: 71616-83-6(Hazardous Substances Data)

Upstream product

• 2234-82-4 1-propylmagnesium chloride 
• 203442-83-5 methyl 4-(N-methoxy-N-methylcarbamoyl)benzoate 
• 67-56-1 methanol 
• 858114-91-7 trifluoromethanesulfonic acid 4-butanoyl-phenyl ester 
• 201230-82-2 carbon monoxide 
• 1571-08-0 methyl 4-formylbenzoate 
• 872254-79-0 4-(1-hydroxybutyl)benzoic acid methyl ester 
• 619-44-3 methyl 4-iodobenzoate 
• 106-37-6 1.4-dibromobenzene 
• 4981-64-0 1-(4-bromophenyl)-1-butanone 
• 1679-64-7 Monomethyl terephthalate 
• 1009-11-6 1-(4-hydroxyphenyl)-butan-1-one 
• 557-93-7 2-bromoprop-1-ene 

Downstream Products

• 872254-79-0 4-(1-hydroxybutyl)benzoic acid methyl ester 
• 71616-82-5 4-butyrylbenzoic acid 
• 1383803-08-4 methyl 3-(4-butyrylbenzamido)propanoate 
• 1393123-89-1 (+/-)-3-(4-(1-(6-(4-phenyl-1H-pyrazol-1-yl)pyridine-3-ylamino)butyl)benzamido)propanoic acid 
• 1393126-67-4 (+/-)-methyl 3-(4-(1-(6-(4-phenyl-1H-pyrazol-1-yl)pyridine-3-ylamino)butyl)benzamido)propanoate 
• 1393124-90-7 (R)-3-(4-(1-(6-(4-phenyl-1H-pyrazol-1-yl)pyridine-3-ylamino)butyl)benzamido)propanoic acid 
• 1393124-89-4 (S)-3-(4-(1-(6-(4-phenyl-1H-pyrazol-1-yl)pyridine-3-ylamino)butyl)benzamido)propanoic acid 
• 1393126-53-8 (+/-)-methyl-4-(1-(3-methyl-4-(4-(trifluoromethyl)-1H-imidazol-1-yl)phenylamino)butyl)benzoate 
• 1421349-08-7 (S)-methyl 4-(1-hydroxybutyl)benzoate 
• 1213123-33-1 (S)-methyl 4-(1-aminobutyl)benzoate 
• 1393126-80-1 (R)-4-(1-hydroxybutyl)benzoic acid 

Relevant articles and documents

Conversion of Aldehydes to Branched or Linear Ketones via Regiodivergent Rhodium-Catalyzed Vinyl Bromide Reductive Coupling-Redox Isomerization Mediated by Formate

A regiodivergent catalytic method for direct conversion of aldehydes to branched or linear alkyl ketones is described. Rhodium complexes modified by PtBu2Me catalyze formate-mediated aldehyde-vinyl bromide reductive coupling-redox isomerization to form branched ketones. Use of the less strongly coordinating ligand, PPh3, promotes vinyl-to allylrhodium isomerization en route to linear ketones. This method bypasses the 3-step sequence often used to convert aldehydes to ketones involving the addition of pre-metalated reagents to Weinreb or morpholine amides.

COMPOUNDS FOR INFLAMMATION AND IMMUNE-RELATED USES

The invention relates to certain compounds or pharmaceutically acceptable salts, solvates, clathrates, or prodrugs thereof, that are useful as immunosuppressive agents and for treating and preventing inflammatory conditions, allergic disorders, and immune disorders

GLUCAGON RECEPTOR MODULATORS

The present invention provides a compound of Formula (I) or a pharmaceutically acceptable salt thereof wherein R1, R2, R3, A1, A2, A3, A4, L, B1, B2, B3 and B4 are as defined herein. The compounds of Formula I have been found to act as glucagon antagonists or inverse agonists. Consequently, the compounds of Formula I and the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucagon.