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6349-98-0

6349-98-0 structure
6349-98-0 structure

Name 2-Phthalimidoglutaric acid
Synonyms N-PHTHALOYL-DL-GLUTAMIC ACID
Glutamic acid, phthalyl
Phthalyl-DL-glutamic Acid
(1)-2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)glutic acid
Einecs -2
2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid
Glutamic acid,phthalyl
2-phthalimido-glutaric acid
Phthalylglutamic acid
2-(1,3-Dioxoisoindolin-2-yl)pentanedioic acid
Pentanedioic acid, 2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)
Phthalimidoglutic acid
Einecs 218-952-2
2-Phthalimidoglutic acid
N,N-phthaloyl-DL-glutamic acid
2-(1,3-Dioxo-1,3-dihydro-2H-isoindole-2-yl)glutic acid
Glutic acid, 2-phthalimido
N-Phthalimido-glutamicacid
2-(1,3-Dihydro-1,3-dioxy-2H-isoindole-2-yl)pentanedioic acid
Phthalyl-DL-glutamicAcid>
N-phthalylglutamic acid
PHTHALOYL-DL-GLUTAMIC ACID
2-(1,3-Dioxo-2,3-dihydro-1H-isoindole-2-yl)pentanedioic acid
Glutic acid, 2-phthalimido-, DL
PHT-DL-GLU-OH
2-PHTHALIMIDINO-GLUTIC ACID
Pomalidomide Impurity 51
2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)glutic acid
Einecs -8
Phthalimidoglutaric acid
Ba 2733
Einecs 228-754-8
Description 2-(1,3-Dioxoisoindolin-2-yl)pentanedioic acid is a glutamic acid derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Melting Point 192 °C
Molecular Formula C13H11NO6
Molecular Weight 277.23000
Exact Mass 277.05900
PSA 111.98000
LogP 0.53850
RTECS MA3810000

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6349-98-0 structure

6349-98-0

Literature: Billman; Harting Journal of the American Chemical Society, 1948 , vol. 70, p. 1473 Full Text View citing articles Show Details King; Kidd Journal of the Chemical Society, 1949 , p. 3315,3318

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6349-98-0 structure

6349-98-0

Literature: Schilling; Strong Journal of the American Chemical Society, 1955 , vol. 77, p. 2843

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6349-98-0 structure

6349-98-0

Literature: King; Kidd Journal of the Chemical Society, 1949 , p. 3315,3318

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6349-98-0 structure

6349-98-0

Literature: Crossley, Maxwell J.; Fung, Yik M.; Kyriakopoulos, Efstathia; Potter, Jeffrey J. Journal of the Chemical Society - Perkin Transactions 1, 1998 , # 6 p. 1123 - 1130

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6349-98-0 structure

6349-98-0

Literature: Du Pont de Nemours and Co. Patent: US2801250 , 1955 ;

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6349-98-0 structure

6349-98-0

Literature: Du Pont de Nemours and Co. Patent: US2801250 , 1955 ;

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6349-98-0 structure

6349-98-0

Literature: Du Pont de Nemours and Co. Patent: US2801250 , 1955 ;

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6349-98-0 structure

6349-98-0

Literature: Du Pont de Nemours and Co. Patent: US2801250 , 1955 ;
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