51600-24-9 Usage
Description
(S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC&, also known as (S)-(-)-α-methyl-1-naphthalenemethylamine, is a chiral amine with the chemical formula C12H13N. It is a white to off-white crystalline powder that is soluble in water and ethanol. (S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is commonly used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. It is also known for its potential as a ligand in asymmetric catalysis, making it a valuable tool in chemical research and development. Additionally, it is used as a reagent in the synthesis of various biologically active compounds and as a precursor in the production of a wide range of chemicals.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for the development of effective and safe drugs and agrochemicals.
Used in Chemical Research and Development:
(S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is used as a ligand in asymmetric catalysis, making it a valuable tool in chemical research and development. Its ability to selectively catalyze reactions can lead to the production of enantiomerically pure compounds, which is essential for the synthesis of biologically active molecules.
Used in Synthesis of Biologically Active Compounds:
(S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is used as a reagent in the synthesis of various biologically active compounds. Its unique structure and properties make it suitable for the development of new drugs and other bioactive molecules with potential therapeutic or agricultural applications.
Used as a Precursor in Chemical Production:
(S)-(-)-1-(1-NAPHTHYL)ETHYLAMINE HYDROC& is used as a precursor in the production of a wide range of chemicals. Its versatility in organic synthesis allows it to be a key component in the manufacturing process of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 51600-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51600-24:
(7*5)+(6*1)+(5*6)+(4*0)+(3*0)+(2*2)+(1*4)=79
79 % 10 = 9
So 51600-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N.ClH/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11;/h2-9H,13H2,1H3;1H/t9-;/m0./s1
51600-24-9Relevant articles and documents
Rhodium-catalyzed asymmetric hydrogenation of unprotected NH imines assisted by a thiourea
Zhao, Qingyang,Wen, Jialin,Tan, Renchang,Huang, Kexuan,Metola, Pedro,Wang, Rui,Anslyn, Eric V.,Zhang, Xumu
supporting information, p. 8467 - 8470 (2014/08/18)
Asymmetric hydrogenation of unprotected NH imines catalyzed by rhodium/bis(phosphine)-thiourea provided chiral amines with up to 97% yield and 95% ee. 1HNMR studies, coupled with control experiments, implied that catalytic chloride-bound intermediates were involved in the mechanism through a dual hydrogen-bonding interaction. Deuteration experiments proved that the hydrogenation proceeded through a pathway consistent with an imine.
