532-24-1

  • Product Name:Tropinone
  • Molecular Formula:C8H13NO
  • Purity:99%
  • Molecular Weight:139.197
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Product Details;

CasNo: 532-24-1

Molecular Formula: C8H13NO

Appearance: white to light yellow crystal powder

Hot Sale low price Best Quality Tropinone 532-24-1

  • Molecular Formula:C8H13NO
  • Molecular Weight:139.197
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.135mmHg at 25°C 
  • Melting Point:40-44 °C(lit.) 
  • Refractive Index:1.4598 (estimate) 
  • Boiling Point:217.1 °C at 760 mmHg 
  • PKA:8.93±0.20(Predicted) 
  • Flash Point:90 °C 
  • PSA:20.31000 
  • Density:1.066 g/cm3 
  • LogP:0.75000 

Tropinone(Cas 532-24-1) Usage

Chemical Properties

Tropinone is a white to light yellow crystal powder, It is an alkaloid and a precursor to a number of additional plant alkaloids. Tropinone is the first intermediate in the biosynthesis of the pharmacologically important tropane alkaloids that possesses the 8-azabicyclo[3.2.1]octane core bicyclic structure that defines this alkaloid class. Chemical synthesis of tropinone was achieved in 1901 but the mechanism of tropinone biosynthesis has remained elusive.

Uses

Tropinone is an oxidative product of Tropane, used to synthesize Morphine and Tropane alkaloids.

Preparation

The first synthesis of tropinone was by Richard Willst?tter in 1901. It started from the seemingly related cycloheptanone, but required many steps and had an overall yield of only 0.75%.Willst?tter had previously synthesized cocaine from tropinone, in what was the first synthesis and elucidation of the structure of cocaine. The 1917 synthesis by Robinson is considered a legend in total synthesis due to its simplicity and biomimetic approach. Tropinone is a bicyclic molecule, but the reactants used in its preparation are fairly simple: succinaldehyde, methyl amine and acetone dicarboxylic acid (or even acetone). The synthesis is a good example of a biomimetic reaction or biogenetic-type synthesis because biosynthesis makes use of the same building blocks. It also demonstrates a tandem reaction in a one-pot synthesis. Furthermore the yield of the synthesis was 17% and with subsequent improvements exceeded 90%.

InChI:InChI=1/C8H13NO/c1-9-6-2-3-7(9)5-8(10)4-6/h6-7H,2-5H2,1H3/p+1/t6-,7+

532-24-1 Relevant articles

-

Polievktov et al.

, (1975)

-

-

Glushkov,R.G. et al.

, (1975)

-

Bioactivity-guided synthesis of tropine derivatives as new agonists for melatonin receptors

Yin, Xiu-Juan,Geng, Chang-An,Huang, Xiao-Yan,Chen, Hao,Ma, Yun-Bao,Chen, Xing-Long,Sun, Chang-Li,Yang, Tong-Hua,Zhou, Jun,Zhang, Xue-Mei,Chen, Ji-Jun

, p. 45059 - 45063 (2016)

Twenty-three tropine derivatives as new ...

METHOD OF PRODUCING TERTIARY AMINE OR TERTIARY AMINE DERIVATIVE

-

Paragraph 0066; 0073; 0079, (2018/10/31)

PROBLEM TO BE SOLVED: To provide a metho...

N-Methylation of Amines with Methanol at Room Temperature

Tsarev, Vasily N.,Morioka, Yuna,Caner, Joaquim,Wang, Qing,Ushimaru, Richiro,Kudo, Akihiko,Naka, Hiroshi,Saito, Susumu

supporting information, p. 2530 - 2533 (2015/05/27)

N-Methylation of amines with methanol pr...

A facile synthesis of enantiopure 7-benzyloxycarbonyl-7-azabicyclo [2.2.1]heptane-2-carboxylic acid

Chiou, Wen-Hua,Chiang, Yu-Min,Chen, Guei-Tang

, p. 92 - 97 (2014/02/14)

An efficient procedure for the preparati...

532-24-1 Process route

3-oxo-tropane-2,4-dicarboxylic acid dimethyl ester
100371-46-8

3-oxo-tropane-2,4-dicarboxylic acid dimethyl ester

(+/-)-2-(carbomethoxy)-3-tropinone
36127-17-0

(+/-)-2-(carbomethoxy)-3-tropinone

tropinone
532-24-1

tropinone

Conditions
Conditions Yield
With phosphate buffer; In water; at 20 ℃; for 24h; pH=8.0;
55%
13%
(1R,3r,5S)-3-tropoyloxytropanium sulfate
55-48-1,300-40-3,620-61-1,1867-24-9,2472-17-5,2623-69-0,14844-27-0,5908-99-6

(1R,3r,5S)-3-tropoyloxytropanium sulfate

tropinone
532-24-1

tropinone

β-Belladonnin
510-25-8,5878-33-1,6696-63-5,23852-32-6

β-Belladonnin

α-Belladonnin
510-25-8,5878-33-1,6696-63-5,23852-32-6

α-Belladonnin

3-tropanol
120-29-6

3-tropanol

pseudotropine
135-97-7

pseudotropine

apoatropine
500-55-0

apoatropine

Conditions
Conditions Yield
In water; for 720h; Irradiation; decomposition in aq. solution; stability after storage in glass and polyethylene containers under various conditions (pH-value, temp., oxidative effects, irradiation);

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