N-Methoxy-N-methylisobutyramide

≥98%

Reagent Code: #217471
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CAS Number 113778-69-1

science Other reagents with same CAS 113778-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.17 g/mol
Formula C₆H₁₃NO₂
badge Registry Numbers
MDL Number MFCD11847606
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

N-Methoxy-N-methylisobutyramide is a Weinreb amide derivative used in organic synthesis for the selective preparation of ketones. It reacts with Grignard reagents or organolithium compounds to form a stable chelated intermediate, which prevents over-addition and allows isolation of the ketone product in high yield. This reagent is valuable in the synthesis of pharmaceutical intermediates and complex bioactive molecules due to its mild conditions, compatibility with sensitive functional groups, and ease of handling.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿440.00
25g
10-20 days ฿8,020.00
100g
10-20 days ฿29,600.00
5g
10-20 days ฿1,680.00
N-Methoxy-N-methylisobutyramide
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N-Methoxy-N-methylisobutyramide is a Weinreb amide derivative used in organic synthesis for the selective preparation of ketones. It reacts with Grignard reagents or organolithium compounds to form a stable chelated intermediate, which prevents over-addition and allows isolation of the ketone product in high yield. This reagent is valuable in the synthesis of pharmaceutical intermediates and complex bioactive molecules due to its mild conditions, compatibility with sensitive functional groups, and ease of h
N-Methoxy-N-methylisobutyramide is a Weinreb amide derivative used in organic synthesis for the selective preparation of ketones. It reacts with Grignard reagents or organolithium compounds to form a stable chelated intermediate, which prevents over-addition and allows isolation of the ketone product in high yield. This reagent is valuable in the synthesis of pharmaceutical intermediates and complex bioactive molecules due to its mild conditions, compatibility with sensitive functional groups, and ease of handling.
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