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1,3-Dioxolane-4-methanol,2,2-diethyl-alpha-propyl-,(alphaR,4S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

444987-65-9

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444987-65-9 Usage

Explanation

The compound's full name, which includes its stereochemistry and classification.

Explanation

The compound belongs to a group of chemical compounds known as dioxolane derivatives.

Explanation

The compound is a colorless liquid that can easily catch fire.

Explanation

The compound has a mild and pleasant smell.

Explanation

The compound is used in the production of various chemicals, including those used in the pharmaceutical, agrochemical, and specialty chemical industries.

Explanation

The compound can act as a solvent in different chemical processes.

Explanation

The compound is known for its high reactivity, making it useful as a starting material in various chemical reactions.

Explanation

The compound may pose certain health and safety risks, so it is important to handle it carefully and follow proper safety protocols.

Class

Dioxolane derivatives

Physical State

Colorless, flammable liquid

Odor

Mild, pleasant

Applications

Pharmaceutical, agrochemical, and specialty chemical production

Solvent

Used for various applications

Reactivity

High

Safety Precautions

Handle with caution due to potential health and safety risks

Check Digit Verification of cas no

The CAS Registry Mumber 444987-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,9,8 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 444987-65:
(8*4)+(7*4)+(6*4)+(5*9)+(4*8)+(3*7)+(2*6)+(1*5)=199
199 % 10 = 9
So 444987-65-9 is a valid CAS Registry Number.

444987-65-9Relevant academic research and scientific papers

Total synthesis of (+)-herbarumin I via intermolecular Nozaki-Hiyama-Kishi reaction

Sabino, Ad?o Aparecido,Pilli, Ronaldo A

, p. 2819 - 2821 (2002)

The phytotoxin herbarumin I, isolated from Phoma herbarum, was stereoselectively synthesized in 17 steps and 6% yield from L-arabinose featuring the intermolecular Nozaki-Hiyama-Kishi coupling and modified Yamaguchi macrolactonization as key steps.

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