成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 120728-10-1 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 120728-10-1
Chemical Structure| 120728-10-1
Structure of 120728-10-1 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 120728-10-1 ]

Related Doc. of [ 120728-10-1 ]

Alternatived Products of [ 120728-10-1 ]
Product Citations

Product Details of [ 120728-10-1 ]

CAS No. :120728-10-1 MDL No. :MFCD02682623
Formula : C10H17NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :ROVVUKFHORPDSM-UHFFFAOYSA-N
M.W : 215.25 Pubchem ID :1512646
Synonyms :

Safety of [ 120728-10-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 120728-10-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 120728-10-1 ]

[ 120728-10-1 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 67-56-1 ]
  • [ 120728-10-1 ]
  • [ 215597-35-6 ]
YieldReaction ConditionsOperation in experiment
75% at 0℃; Reflux Stage 1: Methyl 1-aminocyclobutanecarboxylate
Concentrated H2SO4 (10 ml) was added at 0° C. to a solution of 1-(tert-butoxy-carbonylamino)-cyclobutane-1-carboxylic acid (9.29 mmol, 1 equiv.) in MeOH (30 ml), and the reaction was refluxed for 2 hours at 0° C.
The solvent was removed under reduced pressure.
The residue was taken up in distilled water, adjusted to pH 8-9 with saturated sodium hydrogen carbonate solution and extracted with ethyl acetate (2*200 ml).
The combined organic phases were washed with distilled water (2*150 ml) and saturated NaCl solution (2*50 ml) and dried over sodium sulfate.
The solvent was concentrated under reduced pressure to yield the desired product in the form of a white solid. Yield: 75percent
Reference： [1] Patent: US2010/173889, 2010, A1, . Location in patent: Page/Page column 34
  • 2
  • [ 120728-10-1 ]
  • [ 74-88-4 ]
  • [ 880166-10-9 ]
Reference： [1] Patent: EP1995243, 2008, A1, . Location in patent: Page/Page column 18
  • 3
  • [ 120728-10-1 ]
  • [ 1142211-17-3 ]
Reference： [1] Patent: WO2010/42850, 2010, A1, . Location in patent: Page/Page column 52-53; 67
[2] Patent: WO2011/44501, 2011, A2, . Location in patent: Page/Page column 60; 76
[3] Patent: WO2011/44498, 2011, A1, . Location in patent: Page/Page column 66, 80-81
[4] Patent: WO2011/44538, 2011, A1, . Location in patent: Page/Page column 105-106
[5] Patent: WO2009/67692, 2009, A1, . Location in patent: Page/Page column 187
[6] Patent: WO2010/42851, 2010, A1, . Location in patent: Page/Page column 52-53; 67
[7] Patent: WO2010/132777, 2010, A2, . Location in patent: Page/Page column 195; 48-49
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 120728-10-1 ]

Amino Acid Derivatives

Chemical Structure| 35264-09-6

[ 35264-09-6 ]

1-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid

Similarity: 0.97

Chemical Structure| 123254-58-0

[ 123254-58-0 ]

(R)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid

Similarity: 0.95

Chemical Structure| 151171-11-8

[ 151171-11-8 ]

(S)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid

Similarity: 0.95

Chemical Structure| 252720-31-3

[ 252720-31-3 ]

4-((tert-Butoxycarbonyl)amino)piperidine-4-carboxylic acid

Similarity: 0.93

Chemical Structure| 811460-95-4

[ 811460-95-4 ]

2-((tert-Butoxycarbonyl)amino)-2-cyclobutylacetic acid

Similarity: 0.93

; ;