()-N,N'-Diallyl-L-tartardiamide

98%

Reagent Code: #217801
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CAS Number 58477-85-3

science Other reagents with same CAS 58477-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.25 g/mol
Formula C₁₀H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD00008640
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand or auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its structure supports coordination with metal catalysts, making it valuable in enantioselective transformations such as carbon-carbon bond-forming reactions. Also employed in the development of stereoselective pharmaceutical intermediates where control of chirality is critical. Its diallyl groups can participate in further functionalization or cyclization processes, expanding its utility in synthetic organic chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿580.00
25g
10-20 days ฿5,600.00
100g
10-20 days ฿21,250.00
5g
10-20 days ฿2,210.00
()-N,N'-Diallyl-L-tartardiamide
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Used as a chiral ligand or auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its structure supports coordination with metal catalysts, making it valuable in enantioselective transformations such as carbon-carbon bond-forming reactions. Also employed in the development of stereoselective pharmaceutical intermediates where control of chirality is critical. Its diallyl groups can participate in further functionalization or cyclization processes, expanding its

Used as a chiral ligand or auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its structure supports coordination with metal catalysts, making it valuable in enantioselective transformations such as carbon-carbon bond-forming reactions. Also employed in the development of stereoselective pharmaceutical intermediates where control of chirality is critical. Its diallyl groups can participate in further functionalization or cyclization processes, expanding its utility in synthetic organic chemistry.

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