132487-40-2 Usage
General Description
The chemical compound (1S,2R)-(-)-2-aminocyclohex-3-enecarboxylic acid hydrochloride, also known as tropinone, is a stereochemically pure form of the amino acid derivative cyclohex-3-enecarboxylic acid. Tropinone is a key intermediate in the synthesis of pharmaceuticals and organic compounds, as well as a precursor in the production of atropine and other tropane alkaloids. It is commonly used in the pharmaceutical industry and in organic chemistry research. Tropinone hydrochloride has a wide range of applications, including as a chiral building block in the synthesis of various drugs and bioactive compounds. Additionally, its stereochemically pure form makes it an important tool in asymmetric synthesis and the development of new pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 132487-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132487-40:
(8*1)+(7*3)+(6*2)+(5*4)+(4*8)+(3*7)+(2*4)+(1*0)=122
122 % 10 = 2
So 132487-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2.ClH/c8-6-4-2-1-3-5(6)7(9)10;/h2,4-6H,1,3,8H2,(H,9,10);1H/t5-,6+;/m0./s1
132487-40-2Relevant articles and documents
Stereo- and regiocontrolled syntheses of exomethylenic cyclohexane β-amino acid derivatives
Kiss, Loránd,Forró, Eniko,Orsy, Gy?rgy,ábrahámi, Renáta,Fül?p, Ferenc
, p. 21094 - 21101 (2016/01/25)
Cyclohexane analogues of the antifungal icofungipen [(1R,2S)-2-amino-4-methylenecy clopentanecarboxylic acid] were selectively synthesized from unsaturated bicyclic β-lactams by transformation of the ring olefinic bond through three different regio- and s
Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams
Forro, Eniko,Fueloep, Ferenc
, p. 2875 - 2880 (2007/10/03)
Enantiopure β-amino acids 1a-4a and β-lactams 1b-4b were prepared simultaneously through the lipolase-catalysed enantioselective ring opening of unsaturated racemic β-lactams (±)-1-(±)-4. High enantioselectivities (E>200) were observed when the reactions
