49622-08-4 Usage
Uses
Used in Chemical Synthesis:
Carbamic acid, dimethyl-, chloromethyl ester is used as a reagent in chemical synthesis for the production of various pharmaceuticals and agrochemicals. Its unique properties as a chloromethyl ester derivative of carbamic acid make it a valuable component in the synthesis of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Carbamic acid, dimethyl-, chloromethyl ester is used as an intermediate in the production of various drugs. Its role in the synthesis process is crucial for creating the desired active pharmaceutical ingredients.
Used in Agrochemical Production:
Carbamic acid, dimethyl-, chloromethyl ester is also utilized in the agrochemical industry as an intermediate for the synthesis of various agrochemical products. Its application in this field contributes to the development of effective solutions for agricultural needs.
Check Digit Verification of cas no
The CAS Registry Mumber 49622-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,2 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 49622-08:
(7*4)+(6*9)+(5*6)+(4*2)+(3*2)+(2*0)+(1*8)=134
134 % 10 = 4
So 49622-08-4 is a valid CAS Registry Number.
49622-08-4Relevant academic research and scientific papers
White, Emil H.,Ryan, Thomas J.,Hahn, Bo Sup,Erickson, Ronald H.
, p. 4860 - 4866 (1984)
The synthesis and decomposition of N-(n-butyl)-N',N'-dimethyl-N-nitrosourea (2a), N-(n-butyl)-N',N'-dimethyl-N-nitrourea (3a), N',N'-dimethyl N-(1-norbornyl)-N-nitrosourea (2b), N',N'-dimethyl-N-(1-norbornyl)-N-nitrourea (3b) are described.Several of the compounds show complex NMR spectra ascribable to rotational isomerism.Decomposition of 2a and 3a gave n-butyl N,N-dimethylcarbamate and tetramethylurea, while decompostion of 2b and 3b in methylene chloride gave 1-norbornyl N,N-dimethylcarbamate and 1-norbornyl chloride.These products are formed via diazotic acid derivatives and carbonium ion pairs; the reaction mechanism is essentially the same as that established for the closely related N-nitrosoamides.In concentrated solutions, nitrosourea 2a yielded a new product, amino acid 20.
