6948-55-6 Usage
Uses
Used in Organic Synthesis:
(2Z)-3-(1,3-benzodioxol-5-yl)-2-phenylprop-2-enenitrile is used as a building block in organic synthesis for the production of other chemical compounds. Its unique structure, which includes a benzodioxole ring, a phenyl group, and an unsaturated carbon-carbon double bond, allows for the creation of a variety of complex molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2Z)-3-(1,3-benzodioxol-5-yl)-2-phenylprop-2-enenitrile may be used as a precursor or intermediate in the synthesis of pharmaceutical compounds. Its structural features can be leveraged to develop new drugs with specific therapeutic properties.
Used in Chemical Research:
(2Z)-3-(1,3-benzodioxol-5-yl)-2-phenylprop-2-enenitrile is also used in chemical research to study the properties and reactions of nitriles and unsaturated compounds. This can lead to advancements in understanding chemical reactions and the development of new synthetic methods.
It is important to handle (2Z)-3-(1,3-benzodioxol-5-yl)-2-phenylprop-2-enenitrile with care due to its potential toxicity and health hazards. Proper safety measures should be taken during its production, use, and disposal to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6948-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6948-55:
(6*6)+(5*9)+(4*4)+(3*8)+(2*5)+(1*5)=136
136 % 10 = 6
So 6948-55-6 is a valid CAS Registry Number.
6948-55-6Relevant academic research and scientific papers
Switchable Cobalt-Catalyzed α-Olefination and α-Alkylation of Nitriles with Primary Alcohols
Paudel, Keshav,Xu, Shi,Ding, Keying
supporting information, p. 5028 - 5032 (2021/07/19)
The first switchable α-olefination and α-alkylation of nitriles with primary alcohols catalyzed by a well-defined base transition-metal Co complex was presented. A broad variety of nitriles and primary alcohols are selectively and efficiently converted to the corresponding products by this method. It is noteworthy that the transformation is environmentally benign and atom efficient with H2and H2O being the sole byproducts.
