27675-38-3 Usage
Description
3-METHYL-1-NITROBUT-1-ENE, with the molecular formula C5H9NO2, is a highly reactive and volatile liquid chemical compound. It exhibits a pale yellow color and a distinctive fruity, pungent odor. 3-METHYL-1-NITROBUT-1-ENE is known for its significant role as an intermediate in the synthesis of various products.
Uses
Used in Pharmaceutical Industry:
3-METHYL-1-NITROBUT-1-ENE is used as a key intermediate for the synthesis of several pharmaceuticals. Its reactivity allows it to participate in various chemical reactions, facilitating the production of different medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 3-METHYL-1-NITROBUT-1-ENE serves as an essential intermediate in the creation of various agrochemicals. Its properties make it suitable for use in developing products that can enhance crop protection and management.
Used in Rubber and Plastics Industry:
3-METHYL-1-NITROBUT-1-ENE is also utilized as an intermediate in the production of additives for the rubber and plastics industries. These additives can improve the performance characteristics of the final products, such as durability and flexibility.
Safety Precautions:
Due to its highly flammable nature and potential health hazards, including respiratory system and skin irritation, it is crucial to exercise proper handling and storage measures when working with 3-METHYL-1-NITROBUT-1-ENE. This ensures the safety of individuals and the integrity of the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 27675-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,7 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27675-38:
(7*2)+(6*7)+(5*6)+(4*7)+(3*5)+(2*3)+(1*8)=143
143 % 10 = 3
So 27675-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c1-5(2)3-4-6(7)8/h3-5H,1-2H3/b4-3+
27675-38-3Relevant articles and documents
Effect of the α-alkyl substituent of conjugated nitroolefins on the formation of cyclic nitronic esters vs. nitrocyclopropanes in their reaction with sulfur ylides
Kumaran,Kulkarni
, p. 1545 - 1548 (1995)
The formation of cyclic nitronic esters (isoxazoline N-oxides) vs. nitrocyclopropanes in the reaction of conjugated nitroolefins with sulfur ylides depends on the presence of an α-alkyl substituent in the conjugated nitroolefins.
A Nickel-Bisdiamine Porous Organic Polymer as Heterogeneous Chiral Catalyst for Asymmetric Michael Addition to Aliphatic Nitroalkenes
Buendia, Mikkel B.,Kegn?s, S?ren,Kramer, S?ren
supporting information, p. 5506 - 5512 (2020/10/23)
We report a polystyrene-incorporated chiral nickel(II)-bisdiamine complex, which is accessible on gram-scale. This metal complex functions as a heterogeneous catalyst for the enantioselective Michael addition between malonates and aliphatic nitroalkenes,
CuI-Catalysed Enantioselective Alkyl 1,4-Additions to (E)-Nitroalkenes and Cyclic Enones with Phosphino-Oxazoline Ligands
Shin, Minkyeong,Gu, Minji,Lim, Sung Soo,Kim, Min-Jae,Lee, JuHyung,Jin, HyeongGyu,Jang, Yun Hee,Jung, Byunghyuck
supporting information, p. 3122 - 3130 (2018/07/06)
Catalytic enantioselective conjugate additions of simple alkyl groups to nitroalkenes or cyclic enones that result in the formation of tertiary C–C bonds are described. For these stereoselective addition reactions, new chiral phosphino-oxazoline ligands w
