(2R)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile

95%

Reagent Code: #234622
label
Alias (2S)-N-chloroacetyl-2-cyanotetrahydropyrrolid; S-1-chloroacetyl-2-cyanopyrrolidine; (2S)-1-chloroacetyl-2-cyanopyrrolidine; (2S)-N-chloroacetyl-2-pyrrolidinecarbonitrile; (2S)-N-chloroacetyl-2-pyrrolidinecarbonitrile
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CAS Number 207557-35-5

science Other reagents with same CAS 207557-35-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.61 g/mol
Formula C₇H₉ClN₂O
badge Registry Numbers
MDL Number MFCD08689902
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds for active pharmaceutical ingredients (APIs). Its structure, featuring a chiral pyrrolidine ring with cyano and chloroacetyl groups, supports the development of enantiomerically pure drugs, which are critical in treatments where stereochemistry affects biological activity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its role in constructing pyrrolidine-based nervous system modulators. Also utilized in research settings for developing novel neuroprotective and anticonvulsant molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿154.00
5g
10-20 days ฿159.50
25g
10-20 days ฿670.00
500g
10-20 days ฿10,900.00
100g
10-20 days ฿2,180.00
(2R)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds for active pharmaceutical ingredients (APIs). Its structure, featuring a chiral pyrrolidine ring with cyano and chloroacetyl groups, supports the development of enantiomerically pure drugs, which are critical in treatments where stereochemistry affects biological activity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its role in constructing pyrrolidin

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds for active pharmaceutical ingredients (APIs). Its structure, featuring a chiral pyrrolidine ring with cyano and chloroacetyl groups, supports the development of enantiomerically pure drugs, which are critical in treatments where stereochemistry affects biological activity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its role in constructing pyrrolidine-based nervous system modulators. Also utilized in research settings for developing novel neuroprotective and anticonvulsant molecules.

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