93131-16-9

93131-16-9 structure
93131-16-9 structure
  • Name: Cyclohexanecarboxylic acid-d11
  • Chemical Name: cyclohexanecarboxylic-d11 acid
  • CAS Number: 93131-16-9
  • Molecular Formula: C7HD11O2
  • Molecular Weight: 139.23700
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2016-12-19 14:48:06
  • Modify Date: 2024-02-10 22:11:02
  • Cyclohexanecarboxylic acid-d11 is the deuterium labeled Cyclohexanecarboxylic acid[1]. Cyclohexanecarboxylic acid is a Valproate structural analogue with anticonvulsant action[2].

Name cyclohexanecarboxylic-d11 acid
Synonyms 1,4-[2H10]xylene
(2H10)-p-Xylene
d10-p-xylene
D11 cyclohexanecarboxylic acid
1,4-Di(methyl-d3)benzene-d4
perdeuterocyclohexanecarboxylic acid
Benzene-1,2,4,5-d4-,3,6-di(methyl-d3)
1,4-bis[(2h3)methyl](2h4)benzene
1,4-Dimethylbenzene-d10
p-Xylene-d10
[1,2,2,3,3,4,4,5,5,6,6-2H11]cyclohexanecarboxylic acid
Description Cyclohexanecarboxylic acid-d11 is the deuterium labeled Cyclohexanecarboxylic acid[1]. Cyclohexanecarboxylic acid is a Valproate structural analogue with anticonvulsant action[2].
Related Catalog
In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

[2]. Liu MJ, et al. Pharmacokinetics and pharmacodynamics of valproate analogues in rats. IV. Anticonvulsant action and neurotoxicity of octanoic acid, cyclohexanecarboxylic acid, and 1-methyl-1-cyclohexanecarboxylic acid. Epilepsia. 1994 Jan-Feb;35(1):234-43.  

Molecular Formula C7HD11O2
Molecular Weight 139.23700
Exact Mass 139.15300
PSA 37.30000
LogP 1.65130
Storage condition 2-8°C

~%

93131-16-9 structure

93131-16-9

Literature: Pojer, Peter M. Tetrahedron Letters, 1984 , vol. 25, # 23 p. 2507 - 2508
Precursor  1

DownStream  0