Methyl 4-(chloroformyl)butyrate

CAS : 1501-26-4

Ref. 3D-FM57988

Informations sur le produit

• Nom: Methyl 4-(chloroformyl)butyrate
• Synonymes: Methyl glutaryl chloride, 4-(Carbomethoxy)butanoyl chloride, 4-(Carbomethoxy)butyryl chloride, 4-(Chlorocarbonyl)butanoic acid methyl ester, 4-(Chloroformyl)butyric acid methyl ester, 4-(Methoxycarbonyl)butyryl chloride, 4-Chlorocarbonylbutyric acid methyl ester, 5-Chloro-2-oxopentanoic acid methyl ester, 5-Chloro-5-Oxo-Pentanoicacimethylester, 5-Methoxy-5-oxopentanoyl chloride, 5-chloro-5-OXOPENTANOIC ACID METHYL ESTER, Butyric acid, 4-(chloroformyl)-, methyl ester, Carbomethoxyl Butyryl Chloride, Glutaric acid monomethyl ester chloride, Glutaryl chloride methyl ester, Methyl 4-(Chlorocarbonyl)Butanoate, Methyl 4-(chloroformyl)butanoate, Methyl 5-chloro-5-oxovalerate, Methyl glutaroyl chloride, Monomethyl glutaryl chloride, NSC 93892, Pentanoic acid, 5-chloro-5-oxo-, methyl ester, γ-(Carbomethoxy)butyryl chloride
• CAS: 1501-26-4

Description

Methyl 4-(chloroformyl)butyrate is a synthetic compound that is used in the treatment of depression and microbial infections. It is an inhibitor of glutamate, which is a neurotransmitter that activates the ccr5 receptor on white blood cells. This inhibition prevents the activation of the ccr5 receptor by glutamate and its subsequent entry into the cell. Methyl 4-(chloroformyl)butyrate also has anti-inflammatory effects, which may be due to its ability to inhibit prostaglandin synthesis. The two stereoisomers of methyl 4-(chloroformyl)butyrate are not chemically identical, and this difference can affect their properties and reactivity with other compounds. The analytical methods for these stereoisomers differ, as does their chemical diversity.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 164.59 g/mol
• Formule: C₆H₉ClO₃
• Degré de pureté: Min. 95%
• Couleur/Forme: Colourless To Yellow Liquid
• InChI: InChI=1S/C6H9ClO3/c1-10-6(9)4-2-3-5(7)8/h2-4H2,1H3
• Code InChI: InChIKey=JCAZSWWHFJVFPP-UHFFFAOYSA-N
• SMILES: COC(=O)CCCC(=O)Cl