126760-70-1 Usage
Uses
Used in Fragrance and Flavor Industry:
1-(2,4,6-Trimethylphenyl)-2-nitropropene is used as a key component in the production of fragrances and flavors due to its distinctive sweet, floral scent. Its appealing aroma makes it a popular choice for enhancing the sensory experience of various products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(2,4,6-Trimethylphenyl)-2-nitropropene serves as an essential intermediate in the synthesis of various drugs. Its chemical properties allow for the creation of a range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Chemical Manufacturing:
1-(2,4,6-Trimethylphenyl)-2-nitropropene is also utilized as an intermediate in the manufacture of a variety of chemicals. Its versatility in chemical reactions makes it a valuable asset in the production of different chemical products, further expanding its applications and market value.
Used in Perfumes and Cosmetics:
The sweet, floral scent of 1-(2,4,6-Trimethylphenyl)-2-nitropropene makes it an ideal ingredient for perfumes and cosmetics. Its ability to provide a pleasant and long-lasting fragrance enhances the appeal of these products, making it a sought-after component in the industry.
Check Digit Verification of cas no
The CAS Registry Mumber 126760-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,6 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126760-70:
(8*1)+(7*2)+(6*6)+(5*7)+(4*6)+(3*0)+(2*7)+(1*0)=131
131 % 10 = 1
So 126760-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2/c1-8-5-9(2)12(10(3)6-8)7-11(4)13(14)15/h5-7H,1-4H3/b11-7+
126760-70-1Relevant articles and documents
Porphyrin synthesis from nitrocompounds
Ono, Noboru,Kawamura, Hisayuki,Bougauchi, Masahiro,Maruyama, Kazuhiro
, p. 7483 - 7496 (2007/10/02)
A new porphyrin synthesis starting from nitroalkenes or their equivalents is described. For example, octaethylporphyrin, coproporphyrin, porphyrin-1,2,3,4,5,6,7,8 octapropionic acid, and 2,7,12,17 tetraarylporphyrin are prepared in good yield from readily available materials such as 1-nitropropane, nitroethane, nitromethane, and aldehydes.
