6323-67-7 Usage
Uses
Used in Organic Synthesis:
(1-bromonaphthalen-2-yl)acetonitrile is used as a building block for the preparation of various functionalized naphthalene derivatives. Its unique structure allows for the synthesis of a wide range of organic compounds with potential applications in various industries.
Used in Pharmaceutical Research:
(1-bromonaphthalen-2-yl)acetonitrile is used as a starting material in the development of new pharmaceuticals. Its bromine and nitrile functional groups can be further modified to create novel drug candidates with potential therapeutic benefits.
Used in Material Development:
(1-bromonaphthalen-2-yl)acetonitrile may have potential applications in the development of new materials due to its unique chemical properties. Its bromine atom can be used to introduce new functional groups or to modify existing ones, leading to the creation of materials with specific properties.
Used as a Reagent in Chemical Reactions:
(1-bromonaphthalen-2-yl)acetonitrile can be used as a reagent in various chemical reactions, such as cross-coupling reactions, to form new chemical bonds and create new compounds with desired properties.
Safety Precautions:
Due to its bromine and nitrile functional groups, (1-bromonaphthalen-2-yl)acetonitrile should be handled with caution and proper safety measures to prevent potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 6323-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6323-67:
(6*6)+(5*3)+(4*2)+(3*3)+(2*6)+(1*7)=87
87 % 10 = 7
So 6323-67-7 is a valid CAS Registry Number.
6323-67-7Relevant academic research and scientific papers
Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles
Hsieh, Jen-Chieh,Cheng, An-Yi,Fu, Jun-Hao,Kang, Ting-Wei
supporting information; experimental part, p. 6404 - 6409 (2012/09/05)
An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.
Antihyperglycemic Activity of Novel Naphthalenyl 3H-1,2,3,5-Oxathiadiazole 2-Oxides
Ellingboe, John W.,Lombardo, Louis J.,Alessi, Thomas R.,Nguyen, Thomas T.,Guzzo, Frieda,et al.
, p. 2485 - 2493 (2007/10/02)
A series of naphthalenyl 3H-1,2,3,5-oxathiadiazole 2-oxides was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus.Substitution at the 1-,5-, or 8-positions of the naphthalene ring with a halogen was found to be beneficial to antihyperglycemic activity. 4--3H-1,2,3,5-oxathiadiazole 2-oxide (45), one of the most potent compounds in this series, was selected for further pharmacological evaluation.
α-Aryl-α,α-bis[ω-(disubstituted amino)alkyl]-acetamides
-
, (2008/06/13)
Novel α-aryl-α,α-bis[ω-(disubstituted amino)alkyl]acetamides are described herein. The compounds are useful as anti-arrhythmic agents. The compounds are prepared by reacting an appropriate disubstituted acetonitrile with an appropriate haloalkyl amine and
