3996-15-4 Usage
Description
Sodium formate-D1 is a solid chemical compound that is utilized in a variety of organic reactions and syntheses, making it a valuable component in the field of chemistry.
Uses
Used in Organic Synthesis:
Sodium formate-D1 is used as a reagent for various organic reactions and syntheses, facilitating the formation of complex molecules and structures.
Used in Pharmaceutical Industry:
Sodium formate-D1 is used as a key component in the preparation of [3,2b]pyridines, which are important for the development of new pharmaceutical compounds.
Used in Chemical Research:
In the field of chemical research, sodium formate-D1 is used as a catalyst in the palladium-catalyzed coupling of vinyl triflates with organostannanes, enabling the synthesis of novel organic compounds with potential applications in various industries.
Used in Material Science:
Sodium formate-D1's solid-state properties make it suitable for use in material science, where it can be employed in the development of new materials with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3996-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3996-15:
(6*3)+(5*9)+(4*9)+(3*6)+(2*1)+(1*5)=124
124 % 10 = 4
So 3996-15-4 is a valid CAS Registry Number.
3996-15-4Relevant articles and documents
ENZYME-CATALYZED ORGANIC SYNTHESIS: REGENERATION OF DEUTERATED NICOTINAMIDE COFACTORS FOR USE IN LARGE-SCALE ENZYMATIC SYSNTHESIS OF DEUTERATED SUBSTANCES.
Wong,Whitesides
, p. 5012 - 5014 (2007/10/02)
Procedures were developed for in situ regeneration of deuterated nicotinamide cofactors based on ethanol-1,1,-d//2/alcohol dehydrogenase/aldehyde dehydrogenase, deuterioformate (DCO//2** minus )/formate dehydrogenase, and glycolaldehyde-1,2,2-d//3/aldehyde dehydrogenase. These procedures can be used in the enzyme-catalyzed synthesis of deuterated organic products; representative procedures are illustrated by syntheses of (R)-trifluoroethanol-1-d//1 and L-glutamic alpha -d//1 acid on 0. 1 mol scales. For most synthetic applications, the first of these procedures (CH//3CD//2OH/ADH/AldDH) seems to provide the most practical method for in situ regeneration of deuterated nicotinamide cofactors. The high turnover numbers observed for the nicotinamide cofactors in these syntheses make possible the preparation of deuterated chiral substances with high isotopic purity, regardless of the stereochemistry of the hydride transfers to and from the nicotinamide cofactors.
