1248-42-6 Usage
Description
Methyl 2-[4-[2-piperidinoethoxy]benzoyl]benzoate hydrochloride is a complex organic compound with a unique chemical structure that features a benzoyl group connected to a methyl ester and a piperidinoethoxybenzoyl moiety. methyl 2-[4-[2-piperidinoethoxy]benzoyl]benzoate hydrochloride exhibits a white solid form and possesses specific chemical properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
Methyl 2-[4-[2-piperidinoethoxy]benzoate hydrochloride is used as an antispasmodic agent for its ability to inhibit acetylcholine-induced contractions, similar to the properties of Pitofenone. This makes it a potential candidate for the treatment of various conditions that involve muscle spasms or involuntary contractions.
Used in Drug Combinations:
Methyl 2-[4-[2-piperidinoethoxy]benzoate hydrochloride can be used in combination with other drugs such as Diclofenac, Pitofenone, and Fenpiverinium to enhance antispasmodic activity. This combination may provide a more effective treatment option for patients suffering from muscle spasms or related conditions.
Used in Drug Delivery Systems:
Due to its unique chemical properties, methyl 2-[4-[2-piperidinoethoxy]benzoate hydrochloride may also be utilized in the development of drug delivery systems. These systems can be designed to improve the bioavailability, targeting, and overall efficacy of the compound when used in various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1248-42-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1248-42:
(6*1)+(5*2)+(4*4)+(3*8)+(2*4)+(1*2)=66
66 % 10 = 6
So 1248-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H25NO4.ClH/c1-26-22(25)20-8-4-3-7-19(20)21(24)17-9-11-18(12-10-17)27-16-15-23-13-5-2-6-14-23;/h3-4,7-12H,2,5-6,13-16H2,1H3;1H
1248-42-6Relevant articles and documents
An unexpected reaction of camphor with sodium metal
Khanvilkar, Aditya N.,Gupta, Riddhi,Bedekar, Ashutosh V.
, p. 1327 - 1331 (2016/02/23)
Reaction of camphor with sodium metal at elevated temperature in refluxing THF or toluene, furnishes an unexpected product. The product has been identified by spectral analysis and its structure confirmed by single crystal X-ray diffraction study. A preliminary mechanistic explanation has been suggested to explain this reaction.
Synthesis and characterization of Ru(II) and Ir(III) complexes that bear camphoric 1,3-diamine ligands
Yu, Jun-Lai,Guo, Rong,Wang, Hui,Li, Zhan-Ting,Zhang, Dan-Wei
, p. 36 - 41 (2014/07/22)
Two rigid N-monosulfonylated 1,3-diamine ligands have been prepared starting from commercially available d-camphor through three steps. Their reactions with [Ru(η6-arene)(μ-Cl)Cl]2 (arene = p-cymene or C6H5CO2Et) or [Ir(η 5-C5Me5)(μ-Cl)Cl]2 afforded five new complexes. The structures of one monosulfonamide 1,3-diamine ligand and three organometallic complexes were confirmed by X-ray crystallography.
Synthesis of 1,11,11-trimethyl-3,6-diazotricyclo [6.2.1.0 2,7]undeca-2,6-diene and 1,15,15-trimethyl-3,10-diazotetracyclo[10.2. 1.02,11.04,9]pentadeca-2,4(9),5,7,10-pentaene from camphoroquinone enantiomers
Adamenko,Frolova,Panteleeva,Kuchin
, p. 59 - 62 (2008/02/12)
Optically active camphordihydro-2,3-pyrazine and camphorquinoxaline were prepared from camphoroquinone enantiomers. It was shown that (1S,4R)-(+)-camphoroquinone was formed by oxidation of (1S,3R, 4R)-(-)-3-bromocamphor and (1R,4S)-(-)-camphoroquinone from (1R,3S, 4S)-(+)-3-bromocamphor, respectively. Camphor anhydride was a side product (6-10%) of the reaction. Springer Science+Business Media, Inc. 2007.
