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Chemical Structure| 53838-27-0 Chemical Structure| 53838-27-0

Structure of 53838-27-0

Chemical Structure| 53838-27-0

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Product Details of [ 53838-27-0 ]

CAS No. :53838-27-0
Formula : C10H19NO4
M.W : 217.26
SMILES Code : O=C(OC)[C@@H](N)CCC(OC(C)(C)C)=O
MDL No. :MFCD27578944
InChI Key :JKIPBZRGKFRHKQ-ZETCQYMHSA-N
Pubchem ID :7016385

Safety of [ 53838-27-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 53838-27-0 ]

* 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.

  • Downstream synthetic route of [ 53838-27-0 ]

[ 53838-27-0 ] Synthesis Path-Downstream   1~35

  • 1
  • [ 6233-97-2 ]
  • [ 53838-27-0 ]
  • L-Alanyl-γ-tert.-butyl-L-glutaminsaeure-methylester [ No CAS ]
  • 2
  • [ 6233-97-2 ]
  • [ 53838-27-0 ]
  • [ 53665-73-9 ]
  • 4
  • [ 674-82-8 ]
  • [ 53838-27-0 ]
  • [ 113744-02-8 ]
  • 5
  • [ 1421-69-8 ]
  • [ 53838-27-0 ]
  • Cbz-Gly-Leu-Glu(OtBu)-OMe [ No CAS ]
  • 6
  • [ 58578-45-3 ]
  • [ 53838-27-0 ]
  • methyl 2(S),3'(S)-2-N-(3-benzyloxycarbonylamino-3-benzyloxycarbonylpropyl)amino-4-tert-butoxycarbonylbutanoate [ No CAS ]
  • 7
  • [ 53838-27-0 ]
  • [ 19741-14-1 ]
  • [ 79640-68-9 ]
  • 8
  • [ 53838-27-0 ]
  • [ 1160-54-9 ]
  • Cbz-Gly-Pro-Glu(OtBu)-OMe [ No CAS ]
  • 9
  • [ 2018-66-8 ]
  • [ 53838-27-0 ]
  • [ 26054-96-6 ]
  • 10
  • [ 1738-87-0 ]
  • [ 53838-27-0 ]
  • [ 39802-38-5 ]
  • 11
  • [ 10512-93-3 ]
  • [ 53838-27-0 ]
  • [ 4902-24-3 ]
  • 12
  • [ 53838-27-0 ]
  • [ 33642-47-6 ]
  • Boc-Cys(Trt)-Glu(OtBu)-OMe [ No CAS ]
  • 13
  • [ 53838-27-0 ]
  • [ 146949-07-7 ]
  • (S)-2-(4-Propyl-benzenesulfonylamino)-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • 14
  • [ 75-44-5 ]
  • [ 53838-27-0 ]
  • (S)-2-Isocyanato-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • 15
  • [ 53838-27-0 ]
  • [ 112270-87-8 ]
  • [ 247202-75-1 ]
  • [ 247203-63-0 ]
  • 16
  • [ 53838-27-0 ]
  • C19H21BrO [ No CAS ]
  • 2-{3-[3-(4-<i>tert</i>-butyl-phenoxy)-phenyl]-allylamino}-pentanedioic acid 5-<i>tert</i>-butyl ester 1-methyl ester [ No CAS ]
  • 2-(bis-{3-[3-(4-<i>tert</i>-butyl-phenoxy)-phenyl]-allyl}-amino)-pentanedioic acid 5-<i>tert</i>-butyl ester 1-methyl ester [ No CAS ]
  • 17
  • [ 53838-27-0 ]
  • 4-[3-((E)-3-Bromo-propenyl)-phenoxy]-1,2-dichloro-benzene [ No CAS ]
  • (S)-2-{(E)-3-[3-(3,4-Dichloro-phenoxy)-phenyl]-allylamino}-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • (S)-2-(Bis-{(E)-3-[3-(3,4-dichloro-phenoxy)-phenyl]-allyl}-amino)-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • 18
  • [ 53838-27-0 ]
  • C16H12BrF3O [ No CAS ]
  • (S)-2-{(E)-3-[3-(4-Trifluoromethyl-phenoxy)-phenyl]-allylamino}-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • (S)-2-(Bis-{(E)-3-[3-(4-trifluoromethyl-phenoxy)-phenyl]-allyl}-amino)-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • 19
  • [ 53838-27-0 ]
  • [ 51644-83-8 ]
  • [ 35793-61-4 ]
  • 20
  • [ 53838-27-0 ]
  • [ 418771-11-6 ]
  • (S)-2-[2-((3aR,4S,5aR,9aR,9bR)-2,2,8,8-Tetramethyl-hexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxin-4-yl)-acetylamino]-pentanedioic acid 5-tert-butyl ester 1-methyl ester [ No CAS ]
  • 21
  • [ 53838-27-0 ]
  • [ 123-11-5 ]
  • [ 344765-07-7 ]
  • 22
  • [ 53838-27-0 ]
  • [ 1018929-88-8 ]
YieldReaction ConditionsOperation in experiment
Preparation of alpha-carbonyl guanidine compounds General procedure for solution-phase PyBroP coupling <n="24"/>Carboxylic acid (200-300 mg, 1 eq) and bromo-tris-pyrrolidino- phosphonium hexafluorophosphate (1.1 eq) were suspended in dichloromethane (5 ml_) and the mixture was stirred at 20 0C for 10 minutes. N1N- Diisopropylethylamine (7 eq) was added to the mixture and stirred for a further 10 minutes. Suitably-protected amine (derived from aspartic acid, 1.1 eq) was added and the reaction mixture was then stirred for 2 days at 20 0C. After this time the reaction solvent was removed in vacuo and the residue partitioned between hydrochloric acid (1M aqueous solution, 20 ml_) and ethyl acetate (20 ml_). The phases were separated and the aqueous phase extracted with ethyl acetate (3 x 20 ml_). The organic phases were combined and washed with brine (saturated, aqueous solution, 25 mL), dried over magnesium sulfate, filtered and the solvent removed in vacuo to afford the crude residue.
  • 23
  • [ 908094-01-9 ]
  • [ 2419-56-9 ]
  • [ 53838-27-0 ]
  • 24
  • [ 53838-27-0 ]
  • glycyrrizhin [ No CAS ]
  • [ 948913-76-6 ]
  • 25
  • [ 53838-27-0 ]
  • [ 471-25-0 ]
  • [ 917232-56-5 ]
  • 26
  • [ 53838-27-0 ]
  • [ 917232-60-1 ]
  • 27
  • [ 53838-27-0 ]
  • C47H58N10O12 [ No CAS ]
  • 28
  • [ 53838-27-0 ]
  • [ 917232-57-6 ]
  • 29
  • [ 53838-27-0 ]
  • C54H80N2O22 [ No CAS ]
  • 30
  • [ 53838-27-0 ]
  • (E)-But-2-enoic acid (4-methoxy-benzyl)-((S)-2-oxo-tetrahydro-pyran-3-yl)-amide [ No CAS ]
  • 31
  • [ 53838-27-0 ]
  • [ 489432-92-0 ]
  • 32
  • [ 53838-27-0 ]
  • [ 489432-91-9 ]
  • 33
  • [ 53838-27-0 ]
  • (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-pentanedioic acid 1-methyl ester [ No CAS ]
  • 34
  • [ 53838-27-0 ]
  • [ 489432-90-8 ]
  • 35
  • [ 53838-27-0 ]
  • (S)-2-[((E)-But-2-enoyl)-(4-methoxy-benzyl)-amino]-5-isobutoxycarbonyloxy-5-oxo-pentanoic acid methyl ester [ No CAS ]
 

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