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(R)-N-Glycidylphthalimide

Product Name
(R)-N-Glycidylphthalimide
CAS No.
181140-34-1
Chemical Name
(R)-N-Glycidylphthalimide
Synonyms
Rivaroxaban Impurity M;Rivaroxaban Impurity 84;(R)-GLYCIDYL PHTHALIMIDE;(R)-N-Glycidylphthalimide;N-(R)-Glycidyl Phthalimide;(R)-(-)-GLYCIDYL PHTHALIMIDE;(R)-N-Glycidylphthalimide>Rivaroxaban Impurity 7(R-isomer);(R)-(-)-N-(2,3-Epoxypropyl)pthalaMide;N-((2R)-Oxiran-2-ylmethyl)phthalimide
CBNumber
CB9462849
Molecular Formula
C11H9NO3
Formula Weight
203.19
MOL File
181140-34-1.mol
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(R)-N-Glycidylphthalimide Property

Melting point:
101 °C
Boiling point:
347.4±15.0 °C(Predicted)
Density 
1.446±0.06 g/cm3 (20 ºC 760 Torr)
refractive index 
-10 ° (C=2.2, CHCl3)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
-2.24±0.20(Predicted)
color 
White
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Safety

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
WGK Germany 
2
HS Code 
29251900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H318Causes serious eye damage

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
671711
Product name
(R)-(?)-N-(2,3-Epoxypropyl)phthalimide
Purity
≥99.0% (GC)
Packaging
1g
Price
$40
Updated
2023/06/20
Sigma-Aldrich
Product number
671711
Product name
(R)-(?)-N-(2,3-Epoxypropyl)phthalimide
Purity
≥99.0% (GC)
Packaging
5g
Price
$44
Updated
2023/06/20
TCI Chemical
Product number
G0327
Product name
(R)-N-Glycidylphthalimide
Purity
>99.0%(GC)
Packaging
5g
Price
$60
Updated
2024/03/01
TCI Chemical
Product number
G0327
Product name
(R)-N-Glycidylphthalimide
Purity
>99.0%(GC)
Packaging
25g
Price
$181
Updated
2024/03/01
TRC
Product number
G616005
Product name
N-(R)-GlycidylPhthalimide
Packaging
10g
Price
$145
Updated
2021/12/16
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(R)-N-Glycidylphthalimide Chemical Properties,Usage,Production

Chemical Properties

White solid

Uses

(R)-(-)-N-(2,3-Epoxypropyl)phthalimide may be used in the preparation of the following potential chiral solvating agents:

  • 2-[(2R)-2-hydroxy-3-[[(1R)-2-hydroxy-1-phenyl-ethyl]amino]propyl] isoindoline-1,3-dione
  • 2-[(2R)-2-hydroxy-3-[[(1R,2S)-2-hydroxyindan-1-yl]amino]propyl]isoindoline-1,3-dione
  • 2-[(2R)-2-hydroxy-3-[[(1R)-1-(hydroxymethyl)-propyl]amino]propyl] isoindoline-1,3-dione
  • 2-[(2R)-2-hydroxy-3-[[(1S)-1-phenylethyl]-amino]propyl]isoindoline-1,3-dione
It may also be used in the synthesis of 2-((5R)-2-oxo-5-oxazolidinyl) methyl)-1H-isoindole-1,3 (2H)-dione.

Uses

(R)-N-Glycidylphthalimide is a reagent used for the simultaneous preparation of amino alcohol solvating agents as well as preparation of orally available anticoagulants.

(R)-N-Glycidylphthalimide Preparation Products And Raw materials

Raw materials

Preparation Products

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(R)-N-Glycidylphthalimide Suppliers

Americas 1 Canada 1 China 107 Europe 1 Germany 2 India 6 Japan 6 South Korea 1 Switzerland 1 United Kingdom 2 United States 19 Global 147
Manchester Organics
Tel
--
Fax
--
Email
info@manchesterorganics.com
Country
United Kingdom
ProdList
6834
Advantage
67
Biokemix
Tel
--
Fax
--
Email
info@biokemix.com
Country
United Kingdom
ProdList
1066
Advantage
58
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View Lastest Price from (R)-N-Glycidylphthalimide manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
(R)-N-Glycidylphthalimide 181140-34-1
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-10-19
Zhuozhou Wenxi import and Export Co., Ltd
Product
(R)-()-N-(2,3-Epoxypropyl)phthalimide 181140-34-1
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-06-27
Career Henan Chemical Co
Product
(R)-N-Glycidylphthalimide 181140-34-1
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
200kgs
Release date
2020-01-29

181140-34-1, (R)-N-GlycidylphthalimideRelated Search:

3-Morpholinone, 4-(2,4-diaMinophenyl)- 4-(3-AMino-phenyl)-Morpholin-3-one (R)-5-chloro-N-(4-(3-oxomorpholino)phenyl)-N- ((2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide (S)-2-(3-chloro-2-hydroxypropyl)isoindoline-1,3-dione Rivaroxaban Impurity 93 4-(2-nitrophenyl)Morpholin-3-one Benzoic acid, 2-[[[[(5S)-2-oxo-3-[4-(3-oxo-4-Morpholinyl)phenyl]-5-oxazolidinyl]Methyl]aMino]carbonyl]- 4,5-DICHLOROTHIOPHENE-2-CARBOXYLIC ACID 4-(4-NITROPHENYL)MORPHOLIN-3-ONE (S)-4-(4-(5-(Aminomethyl)-2-oxooxazolidin-3-yl)phenyl)morpholin-3-one.HCl 5-Chloro-2-thiophenecarboxylic Acid 2-Thiophenecarboxylic acid 2-[(2R)-2-Hydroxy-3-[[4-(3-oxo-4-Morpho linyl)phenyl]aMino]propyl]-1H-isoindole-1 ,3(2H)-dione (S)-(+)-Glycidyl Phthalimide (R)-N-Glycidylphthalimide N-(2,3-EPOXYPROPYL)PHTHALIMIDE O-Phthalimide Glycidyl phthalimide

  • (R)-(-)-N-(2,3-Epoxypropyl)phthaliMide, ee: 98%
  • 2-[(2R)-oxiran-2-ylmethyl]-1H-isoindol-1,3(2H)-dione
  • 1H-Isoindole-1,3(2H)-dione,2-[(2R)-2-oxiranylMethyl]-
  • (R)-(-)-N-(2,3-Epoxypropyl)phthaliMide >=99.0% (GC)
  • (R)-2-OXIRANYLMETHYL-ISOINDOLE-1,3-DIONE
  • (R)-(-)-GLYCIDYL PHTHALIMIDE
  • (R)-GLYCIDYL PHTHALIMIDE
  • (R)-(-)-N-(2,3-Epoxypropyl)phthalimide
  • (R)-N-Glycidylphthalimide
  • 2-[(2R)-2-OxiranylMethyl]-1H-isoindol-1,3(2H)-dione
  • (R)-2-(oxiran-2-ylMethyl)isoindoline-1,3-dione
  • 1H-Isoindole-1,3(2H)-dione, 2-[(2R)-oxiranylMethyl]-
  • (R)-2-(Oxiranylmethyl)-1H-isoindole-1,3(2H)-dione
  • (R)-N-(2,3-Epoxypropan-1-yl)phthalimide
  • N-(R)-Glycidyl Phthalimide
  • (R)-(-)-N-(2,3-Epoxypropyl)pthalaMide
  • Rivaroxaban Impurity 7(R-isomer)
  • 2-((2R)-OXIRANYLMETHYL)-1H-ISOINDOLE-1,3(2H)-DIONE
  • Rivaroxaban Impurity M
  • (R)-(-)-N-(2,3-Epoxypropyl)phthalimide, 99%, ee: 98%
  • Rivaroxaban Impurity 84
  • (R)-N-Glycidylphthalimide&gt
  • 2-[[(2R)-oxiran-2-yl]methyl]isoindole-1,3-dione
  • N-((2R)-Oxiran-2-ylmethyl)phthalimide
  • (R)-4-(OXIRAN-2-YLMETHYL)ISOINDOLINE-1,3-DIONE
  • 181140-34-1
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • N-Substituted Phthalimides
  • Oxiranes
  • Simple 3-Membered Ring Compounds