107869-45-4 Usage
Description
(+)-10-CAMPHORSULFONIMINE is a white crystalline solid that serves as a valuable synthetic intermediate in the field of chemistry. It is known for its role in asymmetric hydroxylation, a crucial process in the synthesis of various complex molecules.
Uses
Used in Pharmaceutical Industry:
(+)-10-CAMPHORSULFONIMINE is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its application in asymmetric hydroxylation allows for the creation of chiral molecules with specific configurations, which are essential in the design of effective and selective drugs.
Used in Chemical Synthesis:
In the chemical synthesis industry, (+)-10-CAMPHORSULFONIMINE is utilized as a synthetic intermediate for the production of various complex molecules. Its role in asymmetric hydroxylation enables the synthesis of molecules with specific stereochemistry, which is vital for the development of new materials and compounds with unique properties.
Used in Research and Development:
(+)-10-CAMPHORSULFONIMINE is also employed in research and development settings, where it is used to explore new reaction pathways and develop innovative synthetic methods. Its application in asymmetric hydroxylation can lead to the discovery of novel compounds with potential applications in various fields, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 107869-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,6 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107869-45:
(8*1)+(7*0)+(6*7)+(5*8)+(4*6)+(3*9)+(2*4)+(1*5)=154
154 % 10 = 4
So 107869-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2S/c1-9(2)7-3-4-10(9)6-14(12,13)11-8(10)5-7/h7H,3-6H2,1-2H3/t7-,10-/m0/s1
107869-45-4Relevant articles and documents
Methods and systems for evaluating and predicting the reactivity of monooxygenase enzymes
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Page/Page column 45, (2016/04/20)
Methods and systems for evaluating and predicting the reactivity of natural and engineered monooxygenase enzymes are provided. Methods are provided for acquiring a functional profile (fingerprint) of monooxygenases that encode information regarding the ac
A practical large-scale synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3- ol via asymmetric 1,3-dipolar cycloaddition
Kotian, Pravin L.,Lin, Tsu-Hsing,El-Kattan, Yahya,Chand, Pooran
, p. 193 - 197 (2012/12/24)
(3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol (1), which is a useful intermediate for the synthesis of various bioactive molecules, has been synthesized in 51% overall yield by 1,3-dipolar cycloaddition reaction from the dipolarophile, (E)-3-benzyloxypropenoyl-(2′S)-bornane-10,2-sultam (5), and the achiral ylide precursor, N-(benzyl)-N-(methoxymethyl)-N- (trimethylsilylmethyl)amine (6), without using chromatography and the subsequent reduction with LAH and catalytic hydrogenation. The diastereomers 7 and 8 were separated by crystallization, and efficient procedures were developed for the subsequent reactions to afford 1.
Novel application of chiral micellar media to the Diels-Alder reaction
Diego-Castro, Michael J.,Hailes, Helen C.
, p. 1549 - 1550 (2007/10/03)
A novel chiral surfactant has been used in the first reported aqueous chiral micellar catalysis of a Diels-Alder reaction and enantioselectivities have been observed.
