132431-09-5 Usage
General Description
"(Cbz-4-aminomethyl)piperidine, min. 95%" is a chemical compound that is mainly used in the field of organic chemistry for various research and development purposes. The "min. 95%" indicates that the compound has a minimum purity level of 95%, making it suitable for applications that require high purity. The "Cbz" refers to the carbobenzyloxy protective group, which is commonly used to protect amines in organic synthesis. The 4-aminomethylpiperidine section of the name indicates the existence of a piperidine ring, a common motif in many pharmaceuticals and natural products, which has been functionalized with an aminomethyl group. It is usually utilised in the production of various drugs and is often included in pharmaceutical research. The exact properties of this chemical can vary widely depending on the specific conditions and reactions it is used in.
Check Digit Verification of cas no
The CAS Registry Mumber 132431-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,3 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132431-09:
(8*1)+(7*3)+(6*2)+(5*4)+(4*3)+(3*1)+(2*0)+(1*9)=85
85 % 10 = 5
So 132431-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O2/c17-14(16-10-12-6-8-15-9-7-12)18-11-13-4-2-1-3-5-13/h1-5,12,15H,6-11H2,(H,16,17)
132431-09-5Relevant articles and documents
4-AMINO-BENZAMIDE DERIVATIVES AS 5-HT4 RECEPTOR AGONISTS FOR THE TREATMENT OF GASTROINTESTINAL, NEUROLOGICAL AND CARDIOVASCULAR DISORDERS
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Page/Page column 35, (2010/11/28)
The present invention relates to novel benzamide derivatives of formula (I) having pharmacological activity, to processes for their preparation, to compositions containing them and to their use in the treatment of diseases treatable by 5-HT4 agonism.
Boron trifluoride promoted cleavage of benzyl carbamates
Subhas Bose,Thurston, David E.
, p. 6903 - 6906 (2007/10/02)
A new efficient method for the cleavage of benzyl carbamates (CBZ protective groups) is described that involves a hard acid (BF3·OEt2) - soft nucleophile (EtSH) system. Unlike other available methods, this combination avoids the reduction of olefins, acetylenes, imines, halides and nitro groups, or the possibility of carboxylic ester hydrolysis.