607403-65-6 Usage
Triol
Contains three hydroxyl functional groups
Explanation
A triol is an alcohol with three hydroxyl (-OH) groups attached to the carbon atoms in the molecule.
Explanation
Stereochemistry refers to the spatial arrangement of atoms in a molecule. The (1S,3S) notation indicates the specific configuration of the hydroxyl groups at the 1st and 3rd carbon atoms.
Explanation
1,2,3-Cycloheptanetriol, (1S,3S)(9CI) serves as a key intermediate in the production of various chemicals, including those used in the pharmaceutical and agricultural industries.
Explanation
The compound is also utilized in the production of polymers and resins, which are essential materials in various industries, such as plastics, coatings, and adhesives.
Explanation
The specific arrangement of the hydroxyl groups in 1,2,3-Cycloheptanetriol, (1S,3S)(9CI) plays a crucial role in its reactivity with other molecules and its potential biological activity, making it a valuable molecule in organic synthesis and medicinal chemistry.
Stereochemistry
(1S,3S)
Building block
Used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
Industrial applications
Manufacturing of polymers and resins
Reactivity and biological activity
Determined by precise stereochemistry
Check Digit Verification of cas no
The CAS Registry Mumber 607403-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,4,0 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 607403-65:
(8*6)+(7*0)+(6*7)+(5*4)+(4*0)+(3*3)+(2*6)+(1*5)=136
136 % 10 = 6
So 607403-65-6 is a valid CAS Registry Number.
607403-65-6Relevant articles and documents
Conversion of racemic allylic hydroperoxides into corresponding chiral 1/2,3-triols by using catalytic OsO4 and chiral cinchona ligands in the absence of co-oxidant
G?ksu, Haydar,Gültekin, Mehmet Serdar
, p. 824 - 834 (2015/08/06)
For the first time, removal of oxygen atoms from allylic hydroperoxide functionality and reintroduction to the double bond was achieved using catalytic OsO4 and chiral cinchona alkaloid derivatives in an acetone-water mixture to give corresponding chiral 1/2,3-triol with an enantioselectivity up to 99% ee. The hydroperoxide group was used as both a co-oxidant and a source of hydroxyl groups. This protocol is thought to have potential to provide opportunities for chiral synthesis of 1/2,3-triols from corresponding allylic hydroperoxides in the absence of co-oxidant in one stage for the first time in the literature.
