65481-69-8 Usage
Uses
Used in Organic Synthesis:
2-Aminonorbornane hydrochloride is used as a reagent in organic synthesis for its ability to facilitate the formation of desired products through its reactivity and structural features.
Used as a Chiral Auxiliary:
In the field of asymmetric synthesis, 2-Aminonorbornane hydrochloride is utilized as a chiral auxiliary to assist in the preparation of enantiomerically pure compounds. Its chiral center helps guide the stereoselective formation of target molecules, which is crucial for the development of pharmaceuticals with specific biological activities.
Used as a Resolving Agent:
2-Aminonorbornane hydrochloride serves as a resolving agent for racemic mixtures, enabling the separation of enantiomers. This is important for obtaining pure enantiomers, which can have different biological effects and are often required for drug development.
Used in Pharmaceutical Synthesis:
As a building block, 2-Aminonorbornane hydrochloride is used in the synthesis of pharmaceuticals. Its incorporation into drug molecules can contribute to the development of new medications with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, 2-Aminonorbornane hydrochloride is employed in the synthesis of agrochemicals, potentially leading to the creation of more effective and targeted pesticides or herbicides.
Used in Material Science:
2-Aminonorbornane hydrochloride's applications in material science may involve its use in the development of new materials with specific properties, such as chiral polymers or other advanced materials with unique characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65481-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,8 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65481-69:
(7*6)+(6*5)+(5*4)+(4*8)+(3*1)+(2*6)+(1*9)=148
148 % 10 = 8
So 65481-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N.ClH/c8-7-4-5-1-2-6(7)3-5;/h5-7H,1-4,8H2;1H/t5-,6+,7-;/m1./s1
65481-69-8Relevant academic research and scientific papers
Potential Synthetic Adaptogens: V. Synthesis of Cage Monoamines by the Schwenk–Papa Reaction
Brunilin, R. V.,Mkrtchyan, A. S.,Nawrozkij, M. B.,Novakov, I. A.,Vernigora, A. A.,Voloboev, S. N.,Vostrikova, O. V.
, p. 1742 - 1748 (2020/01/11)
The reduction of cage ketoximes under Schwenk–Papa reaction conditions was studied to establish that the d,l, d- and l-camphor oximes are smoothly reduced to the corresponding amines in high yields. At the same time, d,l-norcamphor and adamantan-2-one oximes undergo partial catalytic deoximation to form a mixture of the corresponding amines and alcohols.
Alkylwanderungen bei Sextettumlagerungen
Langhals, Heinz,Range, Guenter,Wistuba, Eckehardt,Ruechardt, Christoph
, p. 3813 - 3830 (2007/10/02)
The migration aptitude of alkyl groups in the Beckmann-, the Criegee-, and the isonitrile-nitrile rearrangements were investigated.The relative rearrangement rates of substituted benzyl groups are an expression of the charge on the migrating carbon at transition state.From the relative rates of migration of exo- and endo-2-norbornyl groups the geometrical changes at the migrating carbon is estimated.Finally, the different influence of α-branching in the migrating group is discussed for these and some other rearrangements.
