61699-38-5 Usage
Uses
Used in Organic Synthesis:
Cyclooctyl methyl carbonate is used as a solvent for various organic reactions due to its high boiling point and good solubility in organic solvents.
Used in Polymer Production:
Cyclooctyl methyl carbonate is used as a reactive intermediate in the production of polymers, contributing to the formation of desired polymer structures.
Used in Pharmaceutical Industry:
Cyclooctyl methyl carbonate is used as a solvent or intermediate in the synthesis of pharmaceutical compounds, facilitating the production of various medications.
Used in Agrochemical Production:
Cyclooctyl methyl carbonate is used in the synthesis of agrochemicals, such as pesticides and herbicides, to improve their effectiveness and reduce environmental impact.
Used in Industrial Processes:
Cyclooctyl methyl carbonate is used as a versatile compound in various industrial processes due to its relatively low toxicity and minimal environmental impact, making it an attractive choice for many applications.
Check Digit Verification of cas no
The CAS Registry Mumber 61699-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,9 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61699-38:
(7*6)+(6*1)+(5*6)+(4*9)+(3*9)+(2*3)+(1*8)=155
155 % 10 = 5
So 61699-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O3/c1-12-10(11)13-9-7-5-3-2-4-6-8-9/h9H,2-8H2,1H3
61699-38-5Relevant academic research and scientific papers
One-pot carbonyl reduction and carbonate formation using sodium borohydride in dialkyl carbonate solvents
Osumah, Abdulakeem,Magolan, Jakob,Waynant, Kristopher V.
supporting information, (2019/10/14)
Preparation of mixed carbonates proceeded in one step from ketones and aldehydes via treatment with NaBH4 in dimethyl or diethyl carbonate solvent at elevated temperatures. This is an efficient and convenient alternative to the traditional two-step sequence of carbonyl reduction to alcohol and subsequent carbonate formation by treatment with an alkyl chloroformate. 25 examples are presented from 49 to 92% yield, highlighting the versatility of this reaction.
Cycloalkyl carbonates
-
, (2008/06/13)
Carbonic acid esters of the formula STR1 wherein R1 is a member having from 8 to 12 carbon atoms selected from the group consisting of alkylcyclohexyl, alkenylcyclohexyl, alkynylcyclohexyl and cycloalkyl, and R2 is a member selected from the group consisting of alkyl having from 1 to 5 carbon atoms, alkenyl having from 2 to 5 carbon atoms and alkynyl having from 2 to 5 carbon atoms, which compounds have pleasing and persistent scents, as well as processes for producing them and perfume compositions containing them.
