36626-29-6 Usage
Description
(2-CARBOXYETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE, also known as a phosphonium ylide reagent, is a white solid compound with unique chemical properties. It is primarily utilized in the field of organic chemistry for specific reactions, such as Wittig olefinations, where it introduces a carboxylic acid into the molecule. Its structure and reactivity make it a valuable tool for chemists in the synthesis of various complex organic compounds.
Uses
Used in Organic Chemistry:
(2-CARBOXYETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE is used as a reagent for [Wittig olefinations] for [introduction of a carboxylic acid]. This application is particularly relevant in the synthesis of complex organic molecules, where the introduction of a carboxylic acid group is required.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-CARBOXYETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE is used as a key intermediate in the synthesis of various drug molecules. Its ability to introduce a carboxylic acid group during Wittig olefinations makes it a valuable tool for the development of new pharmaceutical compounds with specific therapeutic properties.
Used in Material Science:
(2-CARBOXYETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE is also used in the field of material science for the development of novel materials with unique properties. Its role in the synthesis of complex organic compounds can lead to the creation of new materials with enhanced characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 36626-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36626-29:
(7*3)+(6*6)+(5*6)+(4*2)+(3*6)+(2*2)+(1*9)=126
126 % 10 = 6
So 36626-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H19O2P.ClH/c22-21(23)16-17-24(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20;/h1-15H,16-17H2;1H
36626-29-6Relevant articles and documents
Reaction of 2,3-dihalopropionic acids and their derivatives with P- and N-nucleophiles
Khachikyan,Tovmasyan,Indzhikyan
, p. 1889 - 1894 (2008/02/03)
3-(Triphenylphosphoniochlorido)acrylic and 2,3-dichloropropionic acids react with triphenylphosphine to form 1,2-bis(triphenylphosphoniochlorido) ethane. Under analogous conditions, 2,3-dibromopropionic acid undergoes debromination followed by triphenylphosphine addition to give, after water treatment, 3-(triphenylphosphoniobromido)propionic acid. 2,3- Dihalopropionitriles react similarly, providing 3-(triphenylphosphoniohalido) propionitriles. The reaction of 2,3-dibromopropionamide with triphenylphosphine was performed to show that E-(triphenylphosphoniobromido)acrylic acid is capable, by contrast to what was reported previously, of reacting with triphenylphosphine. Pyridine forms with 2,3-dihalopropionic acids vinylpyridinium halides, while the reactions with aliphatic amines gives rise to dehydrohalogenation products.
SUBSTITUTED DIBENZOXAZEPINE COMPOUNDS
-
, (2008/06/13)
The present invention provides dibenzoxazepine compounds of Formula I: STR1 which are useful as analgesic agents for the treatment of pain, pharmaceutical compositions comprising a therapeutically-effective amount of a compound of Formula I in combination with a pharmaceutically-acceptable carrier, and a method for eliminating or ameliorating pain in an animal comprising administering a therapeutically-effective amount of a compound of Formula I to the animal.
