147102-55-4 Usage
Uses
Used in Organic Synthesis:
1-(3-METHYLPHENYL)-2-NITROPROPENE is used as a reagent in organic synthesis for the preparation of various other compounds. Its unique structure allows for versatile reactions and the creation of a wide range of products.
Used in Chemical Research:
In the field of chemical research, 1-(3-METHYLPHENYL)-2-NITROPROPENE serves as an important compound for studying reaction mechanisms and exploring new synthetic pathways.
Used in Pharmaceutical Synthesis:
1-(3-METHYLPHENYL)-2-NITROPROPENE is used as an intermediate in the synthesis of pharmaceuticals. Its presence in the manufacturing process contributes to the development of new drugs and medications.
Used in Agrochemical Production:
1-(3-METHYLPHENYL)-2-NITROPROPENE is also utilized as an intermediate in the production of agrochemicals, playing a role in the development of pesticides and other agricultural products.
Used in Material Science:
1-(3-METHYLPHENYL)-2-NITROPROPENE is being studied for its potential use as a precursor in the production of materials with specific properties. It may contribute to the development of advanced materials such as conducting polymers and liquid crystals, which have applications in various industries, including electronics and display technology.
Check Digit Verification of cas no
The CAS Registry Mumber 147102-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147102-55:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*2)+(2*5)+(1*5)=104
104 % 10 = 4
So 147102-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO2/c1-8-4-3-5-10(6-8)7-9(2)11(12)13/h3-7H,1-2H3/b9-7+
147102-55-4Relevant academic research and scientific papers
Kawai, Yasushi,Inaba, Yoshikazu,Tokitoh, Norihiro
, p. 309 - 318 (2001)
Various α,β-disubstituted and trisubstituted nitroalkenes were chemoselectively reduced with baker's yeast to the corresponding nitroalkanes. Stereoselectivities of the reduction of α,β-disubstituted nitroalkenes were modest to low, and e.e.s up to 52% were obtained. Trisubstituted nitroalkenes could be reduced to the corresponding nitroalkanes with excellent enantioselectivities, moderate diastereoselectivities and in good yield.
