4417-86-1 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dihydroxy-3,3-dimethylbutanamide is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its unique structure and reactivity to facilitate the creation of new drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-Dihydroxy-3,3-dimethylbutanamide serves as a key intermediate in the production of agrochemicals, contributing to the development of effective compounds for agricultural applications.
Used in Research Applications:
2,4-Dihydroxy-3,3-dimethylbutanamide is utilized in research settings to explore its chemical properties and potential reactions, furthering scientific understanding and innovation in related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4417-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4417-86:
(6*4)+(5*4)+(4*1)+(3*7)+(2*8)+(1*6)=91
91 % 10 = 1
So 4417-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO3/c1-6(2,3-8)4(9)5(7)10/h4,8-9H,3H2,1-2H3,(H2,7,10)/t4-/m0/s1
4417-86-1Relevant academic research and scientific papers
One-pot synthesis of N-substituted pantolactams from pantolactone
Barrios, Ivana,Camps, Pelayo,Comes-Franchini, Mauro,Mu?oz-Torrero, Diego,Ricci, Alfredo,Sánchez, Laura
, p. 1971 - 1979 (2007/10/03)
Rac-N-substituted pantolactams (5) are readily obtained in medium to good yields by reaction of rac-pantolactone (1) with primary amines under acid catalysis, whether at 250°C in a pressure reactor or under microwave irradiation. It appears that the amine can react with pantolactone at the carbonyl carbon atom to give a hydroxyamide (3) in a reversible way and at the methylene carbon atom to give a γ-amino acid (4). The last one on dehydration would give the corresponding pantolactam (5).
A convenient dehydration procedure for the synthesis of enantiomerically pure cyanohydrins
Aquino, Fabrice,Pauling, Horst,Walther, Willy,Plattner, Dietmar A.,Bonrath, Werner
, p. 731 - 737 (2007/10/03)
Starting from protected α-hydroxy amides; cyanohydrins (α-hydroxy nitriles) are obtained through dehydration by cyanuric chloride/DMF in excellent yield. The advantages of the procedure are the extremely mild reaction conditions that prevent racemization.
