112-28-7 Usage
Uses
Used in Coatings Industry:
3-(3-methoxypropoxy)propanol is used as a solvent for its ability to dissolve various materials, enhancing the performance and application of coatings.
Used in Inks Industry:
3-(3-methoxypropoxy)propanol is used as a solvent to improve the flow and application of inks, ensuring consistent color and quality in printing processes.
Used in Cleaners Industry:
3-(3-methoxypropoxy)propanol is used as a solvent to effectively dissolve dirt, grease, and other contaminants, making it a key component in cleaning products.
Used as a Coupling Agent in Industrial Applications:
3-(3-methoxypropoxy)propanol is used to facilitate the mixing of two substances that would not otherwise combine, improving the compatibility and performance of various products.
Used in Environmentally Friendly Products:
3-(3-methoxypropoxy)propanol is used as a low volatility and mild odor solvent, making it a suitable option for products designed to minimize environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 112-28-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112-28:
(5*1)+(4*1)+(3*2)+(2*2)+(1*8)=27
27 % 10 = 7
So 112-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-9-5-3-7-10-6-2-4-8/h8H,2-7H2,1H3
112-28-7Relevant academic research and scientific papers
Reactivity of Neopentyl-Like Compounds in the Synthesis of Branched Polyethers
Dale, Johannes,Fredriksen, Siw B.
, p. 278 - 282 (2007/10/02)
Two singly branched symmetrical hexaethers have been synthesized, starting from 2-bromomethyl-2-methyl-1,3-dibromopropane, in a surprisingly efficient one-pot nucleophilic substitution reaction.It is proposed that the expected adverse neopentyl effect is compensated by favourable neighbouring-group participation involving a 'bromonium'-like four-membered-ring transition state.The corresponding trichloride also reacted cleanly, although much more slowly, while the tritosylate gave an oxetane derivative.
