97384-48-0 Usage
Uses
Used in Detergent Industry:
CitrowanilB is used as a fragrance ingredient for its pleasant, citrus-like aroma, enhancing the overall scent profile of detergents and making them more appealing to consumers.
Used in Soap Industry:
In soap manufacturing, CitrowanilB is utilized as a scent enhancer, providing a long-lasting fragrance that improves the sensory experience of using the soap.
Used in Personal Care Industry:
CitrowanilB is employed as a fragrance ingredient in personal care products, such as lotions, creams, and shampoos, to impart a refreshing and enjoyable citrus scent.
Used as a Stabilizer:
CitrowanilB is used as a stabilizer in various formulations to maintain the integrity and effectiveness of the product over time, preventing degradation and ensuring consistent performance.
Used as a Preservative:
In certain formulations, CitrowanilB functions as a preservative, helping to prevent the growth of microorganisms and extend the shelf life of the products in which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 97384-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,8 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97384-48:
(7*9)+(6*7)+(5*3)+(4*8)+(3*4)+(2*4)+(1*8)=180
180 % 10 = 0
So 97384-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N/c1-3-12(2,10-13)9-11-7-5-4-6-8-11/h3-8H,1,9H2,2H3
97384-48-0Relevant academic research and scientific papers
Indium Tribromide Catalyzed Coupling Reaction of Enol Ethers with Silyl Ketene Imines toward the Synthesis of β,γ-Unsaturated Nitriles
Nishimoto, Yoshihiro,Nishimura, Takashi,Yasuda, Makoto
, p. 18301 - 18308 (2015/12/24)
Herein, a coupling reaction of enol ethers with silyl ketene imines in the presence of catalytic amounts of InBr3 and Me3SiBr is described. Kinetic studies have revealed that an indium catalyst and Me3SiBr accelerated the coupling process and the regeneration of the catalyst, respectively. Various types of enol ethers and silyl ketene imines are applicable. In addition, a formal synthesis of verapamil was achieved by using this novel coupling reaction. Let's get together: The coupling reaction of enol ethers with silyl ketene imines in the presence of a catalytic amount of InBr3 and Me3SiBr is shown (see scheme, TBS=tert-butyl dimethylsilyl). Kinetic studies revealed that an indium salt and Me3SiBr accelerated the coupling process and the regeneration of the catalyst. Several enol ethers and silyl ketene imines are applicable to this strategy.
Alpha-tertiary nitriles
-
, (2008/06/13)
Alpha-tertiary nitriles, a process for making the same, and fragrant substances containing the same, in which the nitriles having the general formula STR1 wherein R1 represents an alkyl radical with 1-3 carbon atoms, R2 and R3/
