32117-82-1 Usage
Uses
Used in Organic Synthesis:
Formamide, N-methoxy-N-methylis used as a solvent and reagent in organic synthesis for its ability to dissolve a wide range of organic compounds and facilitate various chemical reactions.
Used in Pesticide Industry:
Formamide, N-methoxy-N-methylis used as a stabilizer in the production of some pesticides to enhance their effectiveness and prolong their shelf life.
Used in Pharmaceutical Production:
Formamide, N-methoxy-N-methylserves as an intermediate in the manufacturing process of various pharmaceuticals, contributing to the synthesis of active ingredients.
Used in Agrochemical Production:
Formamide, N-methoxy-N-methylis also utilized as an intermediate in the production of agrochemicals, playing a role in the synthesis of substances that protect crops from pests and diseases.
Used in Resin and Coating Industry:
Formamide, N-methoxy-N-methylis used as a softener in the production of resins and coatings, improving their flexibility and performance characteristics.
Used in Adhesive and Sealant Manufacturing:
Formamide, N-methoxy-N-methylis employed in the manufacturing of adhesives and sealants, where it contributes to the formulation of strong, durable, and flexible bonding agents.
It is important to handle Formamide, N-methoxy-N-methylwith care, considering its potential to cause irritation to the skin and respiratory system, as well as its harmful effects on aquatic organisms. Proper safety measures and disposal methods should be followed to minimize environmental and health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 32117-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32117-82:
(7*3)+(6*2)+(5*1)+(4*1)+(3*7)+(2*8)+(1*2)=81
81 % 10 = 1
So 32117-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO2/c1-4(3-5)6-2/h3H,1-2H3
32117-82-1Relevant academic research and scientific papers
Synthesis of silyl formates, formamides, and aldehydesviasolvent-free organocatalytic hydrosilylation of CO2
Ema, Tadashi,Hasegawa, Jun-Ya,Hiyoshi, Mahoko,Murata, Takumi,Ratanasak, Manussada
supporting information, p. 5783 - 5786 (2020/06/03)
Carbon dioxide (CO2) was used as a C1 source to prepare silyl formates, formamides, and aldehydes. Tetrabutylammonium acetate (TBAA) catalyzed the solvent-freeN-formylation of amines with CO2and hydrosilane to give formamides including Weinreb formamide, Me(MeO)NCHO, which was successively converted into aldehydes by one-pot reactions with Grignard reagents.
Reactions of Weinreb amides: formation of aldehydes by Wittig reactions
Hisler, Kevin,Tripoli, Regis,Murphy, John A.
, p. 6293 - 6295 (2007/10/03)
Aldehydes are prepared in excellent yield by Wittig reactions of phosphoranes on the Weinreb amide of formic acid followed by in situ hydrolysis.
Formylations of anions with a 'Weinreb' formamide: N-methoxy-N-methylformamide
Lipshutz, Bruce H.,Pfeiffer, Steven S.,Chrisman, Will
, p. 7889 - 7892 (2007/10/03)
Treatment of organolithiums, Grignard reagents, or enolates with N-methoxy-N-methylformamide leads to formylated products in good yields without competing secondary processes.
