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α,α-dihydroxyl diisopropyl malonate is a sterically hindered di-isopropyl keto malonate hydrate that serves as an excellent N-umpolung reagent for both aliphatic and aromatic primary amines through a simple condensation reaction. Its steric hindrance in the ester moiety allows for the preparation of corresponding iminomalonates in high yield and provides these imines with sufficient hydrolytic stability during the purification process.

70841-85-9

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70841-85-9 Usage

Uses

Used in Organic Synthesis:
α,α-dihydroxyl diisopropyl malonate is used as a reagent for the synthesis of unsymmetrical secondary amines. It acts as a singly N-electrophilic reagent towards strong C-nucleophiles such as alkyland arylmetals (e.g., Grignard reagents), enabling the preparation of these amines at low temperatures and in the absence of transition metal catalysts.
Used in Pharmaceutical Industry:
α,α-dihydroxyl diisopropyl malonate is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of new drugs and drug candidates.
Used in Chemical Research:
α,α-dihydroxyl diisopropyl malonate is used as a research tool in academic and industrial laboratories to study the reactivity and properties of N-umpolung reagents and their applications in organic synthesis and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 70841-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70841-85:
(7*7)+(6*0)+(5*8)+(4*4)+(3*1)+(2*8)+(1*5)=129
129 % 10 = 9
So 70841-85-9 is a valid CAS Registry Number.

70841-85-9Upstream product

70841-85-9Relevant academic research and scientific papers

Facile synthesis of 1,2,3-tricarbonyls from 1,3-dicarbonyls mediated by cerium(IV) ammonium nitrate

Sivan, Akhil,Deepthi, Ani

supporting information, p. 1890 - 1893 (2014/03/21)

A mild and efficient protocol for the synthesis of vicinal tricarbonyl compounds from β-dicarbonyls in a single step using cerium(IV) ammonium nitrate as a catalytic oxidant is described. Ease of execution, wide substrate scope and the suitability for the synthesis of commercially important compounds like ninhydrin, alloxan and oxoline make this reaction particularly noteworthy.

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