154016-57-6 Usage
General Description
3-Bromo-5-(N-BOC)aminomethylisoxazole is a chemical compound with the molecular formula C10H14BrNO4. It is a derivative of isoxazole and contains a bromine atom, a BOC-protected amino group, and a methyl group attached to the isoxazole ring. 3-BROMO-5-(N-BOC)AMINOMETHYLISOXAZOLE is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. It can also serve as a starting material for the synthesis of heterocyclic compounds and other biologically active molecules. 3-Bromo-5-(N-BOC)aminomethylisoxazole has potential applications in the development of new drugs and materials due to its versatile reactivity and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 154016-57-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,1 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154016-57:
(8*1)+(7*5)+(6*4)+(5*0)+(4*1)+(3*6)+(2*5)+(1*7)=106
106 % 10 = 6
So 154016-57-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BrN2O3/c1-9(2,3)14-8(13)11-5-6-4-7(10)12-15-6/h4H,5H2,1-3H3,(H,11,13)
154016-57-6Relevant articles and documents
COMPOUNDS CONTAINING FUSED RINGS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF
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Page/Page column 80, (2011/11/01)
The invention provides novel beta-secretase inhibitors and methods for their use, including methods of treating Alzheimer's disease.
INDOLE OREXIN RECEPTOR ANTAGONISTS
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Page/Page column 33, (2008/06/13)
The present invention is directed to substituted indole compounds which are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved.
Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles: A facile and chemoselective reduction of azide to amino by sodium borohydride using 1,3-propanedithiol as a catalyst
Pei,Wickhan
, p. 7509 - 7512 (2007/10/02)
A series of isoxazole azides were reduced selectively to isoxazole amines in quantitative yield by sodium borohydride using 1,3-propanedithiol as a catalyst.
