6627-68-5 Usage
Structure
A carboxylic acid with a cyclohexene ring and a butyric acid side chain
Usage
In the synthesis of pharmaceuticals and agricultural chemicals, potential applications in the fragrance and flavor industry
Potential properties
Anti-inflammatory and anti-cancer
Physical state
Colorless to pale yellow liquid at room temperature
Storage
Typically stored and handled in a cool, dry environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6627-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6627-68:
(6*6)+(5*6)+(4*2)+(3*7)+(2*6)+(1*8)=115
115 % 10 = 5
So 6627-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H10ClN3OS/c18-13-8-6-11(7-9-13)10-14-16(22)21-15(19-20-17(21)23-14)12-4-2-1-3-5-12/h1-10H/b14-10-
6627-68-5Relevant academic research and scientific papers
SYNTHETIS OF CYCLIC AND ACYCLIC β,γ-UNSATURATED CARBOXYLIC ACIDS VIA AN E1-TYPE IONIZATION/ELIMINATION OF β-LACTONES
Black, T. Howard,Eisenbeis, Shane A.,McDermott, Todd S.,Maluleka, Stephen L.
, p. 2307 - 2316 (2007/10/02)
Cyclic and acyclic ketones were converted in three steps into 3-alkenoic acids, bearing a variety of substituents in the α-position.The sequence, involving ionization/elimination of a β-lactone, affords high yields of pure products uncontaminated with conjugated isomers.Support for an E1-type mechanism is also provided.
A NOVEL SYNTHESIS OF MONO- AND DISUBSTITUTED (1-CYCLOALKENYL) ACETIC ACID DERIVATIVES VIA IONIZATION/ELIMINATION OF β-LACTONES
Black, T. Howard,Eisenbeis, Shane
, p. 2243 - 2248 (2007/10/02)
Spiro β-lactones undergo an ionization/elimination reaction to afford cycloalkenyl acetic acid derivatives in high yield and isomeric purity.
