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(E)-4-benzyloxy-2-nitro-β-pyrrolidinostyrene, with the molecular formula C20H19NO3, is a yellow crystalline solid that serves as a significant building block in organic synthesis and medicinal chemistry. This chemical compound, characterized by the presence of a nitro group and a benzyl ether, is instrumental in creating more complex molecules and holds potential for various applications in the pharmaceutical and agrochemical industries.

99474-22-3

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99474-22-3 Usage

Uses

Used in Pharmaceutical Development:
(E)-4-benzyloxy-2-nitro-β-pyrrolidinostyrene is used as a key intermediate in the synthesis of pharmaceuticals for modulating biological activities. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemicals:
In the agrochemical industry, (E)-4-benzyloxy-2-nitro-β-pyrrolidinostyrene is used as a precursor for the creation of novel compounds with potential applications in pest control and crop protection, contributing to enhanced agricultural productivity.
Safety Note:
Given the potential hazards associated with (E)-4-benzyloxy-2-nitro-β-pyrrolidinostyrene, it is crucial to handle (E)-4-benzyloxy-2-nitro-β-pyrrolidinostyrene with care and adhere to proper safety protocols to minimize risks during its use in research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 99474-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,7 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99474-22:
(7*9)+(6*9)+(5*4)+(4*7)+(3*4)+(2*2)+(1*2)=183
183 % 10 = 3
So 99474-22-3 is a valid CAS Registry Number.

99474-22-3Downstream Products

99474-22-3Relevant academic research and scientific papers

Development of a new linker for the solid-phase synthesis of N-hydroxylated and N-methylated secondary amines

Pauli, Denise,Bienz, Stefan

, p. 1348 - 1356 (2014)

Merrifield resin was modified by the introduction of an ortho-nitrophenylethanal group that served as a linker moiety to attach amines to the resin by reductive amination. Resin-bound tertiary amines were shown to be readily transferred into the respectiv

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