19136-97-1

19136-97-1 structure
19136-97-1 structure
  • Name: 3-Phenyl(2,2-2H2)propanoic acid
  • Chemical Name: hydrocinnamic-2,2-d2 acid
  • CAS Number: 19136-97-1
  • Molecular Formula: C9H8D2O2
  • Molecular Weight: 152.187
  • Catalog: Research Areas Others
  • Create Date: 2018-08-17 01:35:27
  • Modify Date: 2024-01-10 10:10:25
  • Hydrocinnamic acid-d2 is the deuterium labeled Hydrocinnamic acid[1]. Hydrocinnamic acid is the major rhizospheric compound with known growth regulatory activities[2].

Name hydrocinnamic-2,2-d2 acid
Synonyms Benzenepropanoic-α,α-d acid
3-phenylpropionic-2,2-d2 acid
3-Phenyl(2,2-H)propanoic acid
2,2-dideuterio-2-hydroxy-acetic acid
2,2-dideuterio-3-phenylpropanoic acid
Description Hydrocinnamic acid-d2 is the deuterium labeled Hydrocinnamic acid[1]. Hydrocinnamic acid is the major rhizospheric compound with known growth regulatory activities[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]. Tang CS, et al. Collection and Identification of Allelopathic Compounds from the Undisturbed Root System of Bigalta Limpograss (Hemarthria altissima). Plant Physiol. 1982 Jan;69(1):155-60.  

Density 1.1±0.1 g/cm3
Boiling Point 280.0±0.0 °C at 760 mmHg
Molecular Formula C9H8D2O2
Molecular Weight 152.187
Flash Point 170.0±13.9 °C
Exact Mass 152.080627
PSA 37.30000
LogP 1.84
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.542

~61%

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Literature: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION Patent: US2011/224431 A1, 2011 ; Location in patent: Page/Page column 9 ;

~86%

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Literature: Kadam; Desai; Mane Journal of Labelled Compounds and Radiopharmaceuticals, 1999 , vol. 42, # 9 p. 835 - 842

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Literature: Kwart, H.; Brechbiel, M.; Miles, W.; Kwart, L.D. Journal of Organic Chemistry, 1982 , vol. 47, # 23 p. 4524 - 4528

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Literature: MacLean, Micheal J.; Walker, Scott; Wang, Tianfang; Eichinger, Peter C. H.; Sherman, Patrick J.; Bowie, John H. Organic and Biomolecular Chemistry, 2010 , vol. 8, # 2 p. 371 - 377

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Literature: Fu, Tai Y.; Scheffer, John R.; Trotter, James Tetrahedron Letters, 1994 , vol. 35, # 20 p. 3235 - 3238

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Literature: Tordeux, Marc; Marival-Hodebar, Laurence; Pouet, Marie-Josee; Halle, Jean-Claude; Wakselman, Claude Journal of Fluorine Chemistry, 2001 , vol. 111, # 2 p. 147 - 152

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Literature: Maas, Wilfrid P. M.; Veelen, Peter A. van; Nibbering, Nico M. M. Organic Mass Spectrometry, 1989 , vol. 24, p. 546 - 558

~%

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Literature: Maas, Wilfrid P. M.; Veelen, Peter A. van; Nibbering, Nico M. M. Organic Mass Spectrometry, 1989 , vol. 24, p. 546 - 558

~%

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Literature: Maas, Wilfrid P. M.; Veelen, Peter A. van; Nibbering, Nico M. M. Organic Mass Spectrometry, 1989 , vol. 24, p. 546 - 558