504396-87-6 Usage
Molecular structure
The compound consists of a benzene ring with two hydroxyl groups (-OH) attached at the 1 and 3 positions, and a pentyl side chain attached at the 5 position.
Deuterium atoms
The pentyl side chain contains deuterium atoms (2H) at the 4' and 5' positions, which are isotopes of hydrogen with one neutron.
Potential applications
1,3-dihydroxy-5-[4'-(2H2)-5'-(2H3)-pentyl]benzene has potential uses in the pharmaceutical and chemical industries due to its unique structure.
Research interest
The compound's structure may make it of interest for research in drug development or materials science.
Hazards and environmental impact
Its complex structure and potentially unique properties make it important to thoroughly investigate the potential hazards and environmental impact of 1,3-dihydroxy-5-[4'-(2H2)-5'-(2H3)-pentyl]benzene.
Further study needed
Additional study and analysis are required to fully understand the properties and potential applications of this compound.
Functional groups
The compound contains hydroxyl (-OH) functional groups and a pentyl (C5H11) side chain.
Aromaticity
The benzene ring in the compound is aromatic, meaning it has a planar structure with delocalized π electrons.
Stereochemistry
The presence of deuterium atoms at the 4' and 5' positions in the pentyl side chain may introduce stereochemical complexity to the molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 504396-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,4,3,9 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 504396-87:
(8*5)+(7*0)+(6*4)+(5*3)+(4*9)+(3*6)+(2*8)+(1*7)=156
156 % 10 = 6
So 504396-87-6 is a valid CAS Registry Number.
504396-87-6Relevant articles and documents
Synthesis of side chain specifically deuterated (-)-Δ9-tetrahydrocannabinols
Nikas, Spyros P.,Thakur, Ganesh A.,Makriyannis, Alexandros
, p. 1065 - 1076 (2007/10/03)
(-)-Δ9-Tetrahydrocannabinols specifically deuterated at the n-pentyl side chain were prepared using the corresponding resorcinols as key intermediates. To obtain the deuterated resorcinols we developed conditions under which no deuterium scramb
