844-44-0 Usage
Uses
Used in Organic Synthesis:
(4-chlorophenyl)[(4Z)-4-(hydroxyimino)-3-methoxycyclohexa-2,5-dien-1-ylidene]acetonitrile is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for a range of chemical reactions, making it a valuable component in the creation of new molecules with specific properties and applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-chlorophenyl)[(4Z)-4-(hydroxyimino)-3-methoxycyclohexa-2,5-dien-1-ylidene]acetonitrile is used as a key compound in the development of new drugs. Its structural features may contribute to the design of novel therapeutic agents, potentially leading to the discovery of innovative treatments for various medical conditions.
Used in Material Development:
(4-chlorophenyl)[(4Z)-4-(hydroxyimino)-3-methoxycyclohexa-2,5-dien-1-ylidene]acetonitrile's unique properties also make it a candidate for use in the development of new materials. Its potential applications in this field could include the creation of advanced materials with specific characteristics, such as improved strength, durability, or chemical resistance.
Used as a Reagent in Chemical Reactions:
(4-chlorophenyl)[(4Z)-4-(hydroxyimino)-3-methoxycyclohexa-2,5-dien-1-ylidene]acetonitrile can be employed as a reagent in various chemical reactions, facilitating the synthesis of other compounds or aiding in the modification of existing molecules. Its versatility in this context makes it a valuable tool for researchers and chemists working in a range of industries.
Check Digit Verification of cas no
The CAS Registry Mumber 844-44-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 844-44:
(5*8)+(4*4)+(3*4)+(2*4)+(1*4)=80
80 % 10 = 0
So 844-44-0 is a valid CAS Registry Number.
844-44-0Relevant academic research and scientific papers
Solvent-free mechanochemical synthesis of arylcyanomethylenequinone oximes from phenylacetonitriles and 4-unsubstituted nitroaromatic compounds using KF/nano-γ-Al2O3 as catalyst
Hong, Zhi,Li, Jian-Jun,Chen, Guang,Jiang, Hua-Jiang,Yang, Xiao-Feng,Pan, Heng,Su, Wei-Ke
, p. 13581 - 13588 (2016/02/12)
Solvent-free condensation of phenylacetonitriles with 4-unsubstituted nitroaromatic compounds to produce a series of arylcyanomethylenequinone oximes was described in the presence of KF/nano-γ-Al2O3 under high-speed vibration milling
