730964-86-0 Usage
Description
D,L-3-ISOCYANO-N-BUTYRIC ACID METHYL ESTER is a chemical compound characterized by the molecular formula C7H11NO3. It is a methyl ester derivative of isocyanobutyric acid, known for its applications in the synthesis of pharmaceuticals, agrochemicals, and other industrial products such as polymers.
Used in Pharmaceutical Industry:
D,L-3-ISOCYANO-N-BUTYRIC ACID METHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and improve existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, D,L-3-ISOCYANO-N-BUTYRIC ACID METHYL ESTER is utilized as a precursor in the production of agrochemicals, which are essential for enhancing crop protection and yield.
Used in Polymer Production:
D,L-3-ISOCYANO-N-BUTYRIC ACID METHYL ESTER is also employed in the manufacturing process of polymers, where it plays a role in creating materials with specific properties for various applications.
Safety Note:
It is crucial to handle D,L-3-ISOCYANO-N-BUTYRIC ACID METHYL ESTER with care, as it can be an irritant to the skin, eyes, and respiratory system. Adhering to proper safety procedures is essential to minimize potential health risks during its use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 730964-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,0,9,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 730964-86:
(8*7)+(7*3)+(6*0)+(5*9)+(4*6)+(3*4)+(2*8)+(1*6)=180
180 % 10 = 0
So 730964-86-0 is a valid CAS Registry Number.
730964-86-0Relevant articles and documents
Pathway from N-Alkylglycine to Alkylisonitrile Catalyzed by Iron(II) and 2-Oxoglutarate-Dependent Oxygenases
Chang, Wei-chen,Chen, Jinfeng,Chen, Tzu-Yu,Guo, Yisong,Tang, Yijie,Zhou, Jiahai
supporting information, p. 7367 - 7371 (2020/03/13)
N-alkylisonitrile, a precursor to isonitrile-containing lipopeptides, is biosynthesized by decarboxylation-assisted -N≡C group (isonitrile) formation by using N-alkylglycine as the substrate. This reaction is catalyzed by iron(II) and 2-oxoglutarate (Fe/2OG) dependent enzymes. Distinct from typical oxygenation or halogenation reactions catalyzed by this class of enzymes, installation of the isonitrile group represents a novel reaction type for Fe/2OG enzymes that involves a four-electron oxidative process. Reported here is a plausible mechanism of three Fe/2OG enzymes, Sav607, ScoE and SfaA, which catalyze isonitrile formation. The X-ray structures of iron-loaded ScoE in complex with its substrate and the intermediate, along with biochemical and biophysical data reveal that -N≡C bond formation involves two cycles of Fe/2OG enzyme catalysis. The reaction starts with an FeIV-oxo-catalyzed hydroxylation. It is likely followed by decarboxylation-assisted desaturation to complete isonitrile installation.
