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tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate

Product Name
tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate
CAS No.
558442-96-9
Chemical Name
tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate
Synonyms
105471;tert-butyl N-(4-morpholinocyclohexyl)carbamate;tert-Butyl (trans-4-morpholinocyclohexyl)carbamate;tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate;Carbamic acid, N-[trans-4-(4-morpholinyl)cyclohexyl]-, 1,1-dimethylethyl ester
CBNumber
CB52684445
Molecular Formula
C15H28N2O3
Formula Weight
284.39
MOL File
558442-96-9.mol
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tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate Property

Boiling point:
396.3±37.0 °C(Predicted)
Density 
1.07±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
12.50±0.40(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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

Matrix Scientific
Product number
120887
Product name
tert-Butyl((1r,4r)-4-morpholinocyclohexyl)-carbamate
Purity
97%
Packaging
5g
Price
$1486
Updated
2021/12/16
Matrix Scientific
Product number
120887
Product name
tert-Butyl((1r,4r)-4-morpholinocyclohexyl)-carbamate
Purity
97%
Packaging
10g
Price
$2376
Updated
2021/12/16
Ambeed
Product number
A123528
Product name
tert-Butyl(trans-4-morpholinocyclohexyl)carbamate
Purity
95+%
Packaging
100mg
Price
$89
Updated
2021/12/16
Ambeed
Product number
A123528
Product name
tert-Butyl(trans-4-morpholinocyclohexyl)carbamate
Purity
95+%
Packaging
250mg
Price
$111
Updated
2021/12/16
Crysdot
Product number
CD11104477
Product name
tert-Butyl(trans-4-morpholinocyclohexyl)carbamate
Purity
95+%
Packaging
1g
Price
$294
Updated
2021/12/16
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tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate Chemical Properties,Usage,Production

Synthesis

5414-19-7

177906-48-8

558442-96-9

The general procedure for the synthesis of tert-butyl (trans-4-morpholinocyclohexyl)carbamate from 2,2'-dibromodiethyl ether and tert-butyl trans-(4-aminocyclohexyl)carbamate was as follows: 21.43 g (0.1 mol) of tert-butyl N-(trans-4-aminocyclohexyl)carbamate was dissolved into 250 mL of N,N-dimethylformamide, followed by addition of 16.76 mL (0.12 mol) bis(2-bromoethyl) ether and 34.85 mL (0.25 mol) triethylamine. The reaction mixture was stirred at 70°C for 6 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate, and the organic layer was washed sequentially with aqueous sodium carbonate and saturated brine solution, and then dried over anhydrous sodium sulfate. The solvent was again removed by reduced pressure distillation and the residue was purified by silica gel column chromatography (elution gradient: from pure chloroform to chloroform/methanol=30/1) to give 19.92 g (70% yield) of tert-butyl (trans-4-morpholino cyclohexyl)carbamate.

References

[1] Patent: EP1775298, 2007, A1. Location in patent: Page/Page column 33-34

tert-butyl ((1r,4r)-4-Morpholinocyclohexyl)carbaMate Preparation Products And Raw materials

Raw materials

Preparation Products

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