61299-72-7 Usage
Description
Pinane-3-(methylamine) is a chemical compound with the molecular formula C10H21N. It is a derivative of pinane, a bicyclic hydrocarbon, with a methylamine functional group attached to the third carbon of the pinane ring. pinane-3-(methylamine) is characterized by its unique chemical structure and has diverse applications across various industries.
Uses
Used in Pharmaceutical and Agrochemical Industries:
Pinane-3-(methylamine) is used as a precursor for the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a key building block in the development of new drugs and agricultural products.
Used in Organic Chemistry:
Pinane-3-(methylamine) serves as a versatile building block for the preparation of different organic compounds. Its functional group can be further modified or used in reactions to create a variety of organic molecules.
Used in Fragrance and Flavoring Agent Production:
Due to its unique chemical structure, pinane-3-(methylamine) is also used in the production of fragrances and flavoring agents. Its properties contribute to the creation of distinct scents and tastes in various consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 61299-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,9 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61299-72:
(7*6)+(6*1)+(5*2)+(4*9)+(3*9)+(2*7)+(1*2)=137
137 % 10 = 7
So 61299-72-7 is a valid CAS Registry Number.
61299-72-7Relevant articles and documents
Regeneration of 6-fluoro-4-chromanone from by-products in the synthesis of sorbinil
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, (2008/06/13)
6-Fluoro-4-chromanone, a sorbinil intermediate, is regenerated from enantiomeric and mixtures of enantiomeric and racemic compounds obtained as major by-products in the synthesis of sorbinil. The regenerated intermediate is useful in the synthesis of additional sorbinil.
Resolution of racemic pantolactone
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, (2008/06/13)
A process for resolving racemic α-hydroxy-β,β-dimethyl-γ-butyrolactone, referred to as D,L-pantolactone, into its optical antipodes, based on the separation of diastereomeric salts of D,L-pantoic acid (α,γ-dihydroxy-β,β-dimethylbutyric acid), produced from D,L-pantolactone, by means of (-)-3-aminomethylpinane, (+)-3-aminomethylpinane or one of their acid addition salts, as a new resolving agent.