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125630-28-6

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125630-28-6 Usage

Chemical Properties

Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 125630-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,6,3 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125630-28:
(8*1)+(7*2)+(6*5)+(5*6)+(4*3)+(3*0)+(2*2)+(1*8)=106
106 % 10 = 6
So 125630-28-6 is a valid CAS Registry Number.

125630-28-6Relevant articles and documents

Imine salt derivative, preparation method thereof and preparation method of nicotine

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Paragraph 0089-0091; 0093, (2020/01/12)

The invention discloses an imine salt derivative, a preparation method thereof and a preparation method of nicotine. The preparation method of nicotine includes the steps of: adding an imine salt derivative shown as general formula (I) or (II) in the specification and a reducing agent into a solvent for reaction to prepare a racemic nicotine solution; adding a second quenching agent into the racemic nicotine solution to obtain a nicotine precursor solution; and adding an extracting agent into the nicotine precursor solution, conducting reduced pressure concentration, and performing drying andremoving the solvent, thus obtaining nicotine. According to the invention, through the imine salt derivative intermediate synthesized for the first time and the use of the cheap reducing agent, the intermediate is reduced under a relatively mild condition to obtain racemic nicotine. Compared with the existing nicotine synthesis process, the method has the advantages of mild synthesis process conditions, simple equipment requirement, high product purity and high synthesis rate, and is particularly suitable for industrial production.

A chemo-enzymatic route to enantiomerically pure cyclic tertiary amines

Dunsmore, Colin J.,Carr, Reuben,Fleming, Toni,Turner, Nicholas J.

, p. 2224 - 2225 (2007/10/03)

Deracemization of racemic chiral tertiary amines has been achieved by combination of an enantioselective amine oxidase, obtained through directed evolution, and ammonia borane in a one-pot process. Copyright

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