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Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI)

Product Name
Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI)
CAS No.
511254-92-5
Chemical Name
Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI)
Synonyms
Alfacalcidol Impurity 12;(2S)-1-BENZYL-2-METHYLPIPERAZINE;(S)-1-Benzyl-2-methylpiperazine - [B91459];Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)-;Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI)
CBNumber
CB31065342
Molecular Formula
C12H18N2
Formula Weight
190.28
MOL File
511254-92-5.mol
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Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI) Property

Boiling point:
282℃
Density 
0.991
Flash point:
112℃
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
9.29±0.40(Predicted)
Appearance
Brown to dark brown Liquid
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Safety

HS Code 
2933599590
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FB140528
Product name
(S)-1-Benzyl-2-methylpiperazine
Packaging
250mg
Price
$72.5
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB140528
Product name
(S)-1-Benzyl-2-methylpiperazine
Packaging
500mg
Price
$125
Updated
2021/12/16
Activate Scientific
Product number
AS41130
Product name
(S)-1-Benzyl-2-methylpiperazine
Purity
95% ee
Packaging
1g
Price
$169
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB140528
Product name
(S)-1-Benzyl-2-methylpiperazine
Packaging
1g
Price
$217
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB140528
Product name
(S)-1-Benzyl-2-methylpiperazine
Packaging
2g
Price
$377
Updated
2021/12/16
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Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI) Chemical Properties,Usage,Production

Synthesis

716339-52-5

511254-92-5

Step 2: tert-Butyl (S)-4-benzyl-3-methylpiperazine-1-carboxylate (11.6 g, 40 mmol) was dissolved in dichloromethane (100 mL), trifluoroacetic acid (20 mL) was added slowly and the reaction mixture was stirred at room temperature for 30 minutes. Upon completion of the reaction, the reaction solution was concentrated to remove the solvent. Subsequently, the concentrate was dissolved in ice water and concentrated sodium hydroxide solution was added in batches to adjust the pH to above 13. The aqueous phase was extracted with ethyl acetate, the organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated to afford (S)-1-benzyl-2-methylpiperazine (6.84 g, 90% yield), which could be used in the next reaction without further purification. Mass spectrum (ESI) m/z: 191.2 [M+H]+.

References

[1] Organic Letters, 2008, vol. 10, # 7, p. 1473 - 1476
[2] Patent: US2004/132711, 2004, A1. Location in patent: Page/Page column 16-17
[3] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0133
[4] Patent: US2009/270336, 2009, A1. Location in patent: Page/Page column 11-12
[5] Patent: US2005/261310, 2005, A1. Location in patent: Page/Page column 12-13; 29

Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI) Preparation Products And Raw materials

Raw materials

Preparation Products

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Piperazine, 2-methyl-1-(phenylmethyl)-, (2S)- (9CI) Suppliers

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