190067-87-9 Usage
Chemical structure
A complex chemical compound with a 1,3-pentanediol backbone and additional groups attached to it.
Components
Contains a dioxolane ring, a methylene group, and a phenylmethoxy group.
Physical state
A colorless liquid.
Industrial applications
Used as a solvent, a chemical intermediate, and in the production of polymers.
Unique structure
The compound's structure and properties make it useful in a wide range of industries.
Industries served
Pharmaceutical, cosmetics, and adhesives industries.
Solvent properties
Due to its ability to dissolve a variety of substances, it is used as a solvent in various chemical processes.
Chemical intermediate
Acts as a precursor in the synthesis of other complex molecules.
Polymer production
Used in the production of polymers due to its ability to form covalent bonds with other monomers.
Safety considerations
As with any chemical compound, it is important to follow proper handling and storage procedures to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 190067-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,0,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 190067-87:
(8*1)+(7*9)+(6*0)+(5*0)+(4*6)+(3*7)+(2*8)+(1*7)=139
139 % 10 = 9
So 190067-87-9 is a valid CAS Registry Number.
190067-87-9Relevant academic research and scientific papers
The synthesis of the zaragozic acids: Equilibrium control of stereochemistry in the dioxabicyclo[3.2.1]octane core
Hegde, Sayee G.,Myles, David C.
, p. 4329 - 4332 (2007/10/03)
The synthesis of the core of zaragozic acid Bx3 and a general strategy for the synthesis of the dioxabicyclo[3.2.1] octane core of the zaragozic acids is described.
An improved procedure for the preparation of the O,2-dianion of allyl alcohol
Hegde, Sayee G.,Myles, David C.
, p. 2111 - 2115 (2007/10/03)
An improved procedure for the preparation of the O,2-dianion of allyl alcohol is described. The use of the magnesium alkoxide of 2-bromopropen-1- ol instead of the known lithium salt, suppresses dehydrohalogenation upon treatment with tert-butyl lithium a
