51300-90-4 Usage
Uses
Used in Organic Synthesis:
Tert-butyl hydrogen carbonate is used as a reagent in organic synthesis for its high reactivity and stability, enabling the production of a wide range of chemical compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, tert-butyl hydrogen carbonate is used as an intermediate in the synthesis of various drugs, contributing to the development of new medications and improving the efficiency of existing ones.
Used in Pesticide Production:
Tert-butyl hydrogen carbonate is utilized as an intermediate in the production of pesticides, helping to create effective and safe agricultural chemicals for crop protection.
Used in Polymer and Resin Manufacturing:
As a solvent, tert-butyl hydrogen carbonate is used in the manufacturing of polymers and resins, enhancing the properties and performance of these materials in various applications.
Used in Chemical Industry:
Tert-butyl hydrogen carbonate is employed as a versatile and valuable chemical in the industry, serving as a key component in the synthesis of a wide range of chemical products and contributing to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 51300-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51300-90:
(7*5)+(6*1)+(5*3)+(4*0)+(3*0)+(2*9)+(1*0)=74
74 % 10 = 4
So 51300-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c1-5(2,3)8-4(6)7/h1-3H3,(H,6,7)
51300-90-4Relevant academic research and scientific papers
CONTRASTERIC CARBOXIMIDE HYDROLYSIS WITH LITHIUM HYDROPEROXIDE
Evans, David A.,Britton, Thomas C.,Ellman Jon A.
, p. 6141 - 6144 (2007/10/02)
The use of lithium hydroperoxide for the highly regioselective hydrolysis of a range of carboximides is described.Numerous cases are provided where the regioselectivities exhibited by this reagent are dramatically different than the complementary reactions with hydroxide.
