16777-87-0 Usage
Description
3,3-Diethoxy-1-propanol is an organic compound with the molecular formula C7H16O3. It is a colorless liquid that is soluble in water and has a sweet taste. 3,3-DIETHOXY-1-PROPANOL is characterized by its three ethoxy groups attached to a propane backbone, which gives it unique chemical properties and makes it a versatile building block in various chemical reactions.
Uses
Used in Chemical Synthesis:
3,3-Diethoxy-1-propanol is used as a synthetic intermediate for the production of various chemicals and materials. Its ability to react with other compounds makes it a valuable component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,3-Diethoxy-1-propanol is used as a building block for the synthesis of various drugs and drug candidates. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Polymer Synthesis:
3,3-Diethoxy-1-propanol is used as a monomer in the synthesis of polymers, such as α-acetal-poly(ethylene glycol), which has potential applications in various fields, including drug delivery and material science. The reaction with potassium napthalide and ethylene oxide inside an UniLab Glovebox allows for the controlled synthesis of this polymer.
Check Digit Verification of cas no
The CAS Registry Mumber 16777-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,7 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16777-87:
(7*1)+(6*6)+(5*7)+(4*7)+(3*7)+(2*8)+(1*7)=150
150 % 10 = 0
So 16777-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-3-9-7(5-6-8)10-4-2/h7-8H,3-6H2,1-2H3
16777-87-0Relevant articles and documents
Method For Manufacturing Hydroxyl Group-containing Acetal Compound
-
Page/Page column 5, (2012/11/08)
A method for manufacturing an acetal compound represented by the formula [1] in which the steps (A) to (D) as defined herein are performed sequentially, and an acetal compound of the formula [1] which is produced by the method: wherein n is 0 or 1 provided that R1 groups may be bonded or may not be bonded to each other when n is 0; R1 is an alkyl group having 1 or 2 carbon atoms or an alkylene group having 1 or 2 carbon atoms and the R1 groups may be same or different from each other; and R2 is an alkylene group having 1 or 6 carbon atoms.
TOTAL SYNTHESIS OF MAYTANSINOIDS. APPROACH TO 4,6-BISDEMETHYLMAYTANSINE AND 4-DEMETHYLMAYTANSINE
Benechie, Michel,Delpech, Bernard,Khuong-Huu, Qui,Khuong-Huu, Francoise
, p. 1895 - 1910 (2007/10/02)
A convergent strategy was elaborated to synthesize maytansine 1 and maytansinoids modified on the carbon skeleton, especially 4-demethylmaytansine 2, 6-demethylmaytansine 3, 4,6-bisdemethylmaytansine 4.In this paper, the feasibility of the project was verified by the preparation of key intermediates for the synthesis of 4,6-bisdemethylmaytansine and 6-demethylmaytansine.The C-1-N open chain compound 18 in the 4,6-bisdemethyl series was obtained.
Thiazolidinylethylchlorocarbonates
-
, (2008/06/13)
This invention relates to 2-(thiazolidin-2'-yl) ethylchlorocarbonates useful as intermediates in the synthesis of photographic image dye-providing materials and to their preparation by the reaction of the appropriate 2-(2'-hydroxyethyl)-thiazolidine with phosgene under certain conditions.
