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Chemical Structure| 32991-17-6 Chemical Structure| 32991-17-6
Chemical Structure| 32991-17-6

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Product Details of (tert-Butoxycarbonyl)-L-leucylglycine

CAS No. :32991-17-6
Formula : C13H24N2O5
M.W : 288.34
SMILES Code : O=C(O)CNC([C@@H](NC(OC(C)(C)C)=O)CC(C)C)=O
MDL No. :MFCD00076954
InChI Key :NRXDUMDULDHIEA-VIFPVBQESA-N
Pubchem ID :7018768

Safety of (tert-Butoxycarbonyl)-L-leucylglycine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of (tert-Butoxycarbonyl)-L-leucylglycine

* 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 [ 32991-17-6 ]

[ 32991-17-6 ] Synthesis Path-Downstream   1~35

  • 1
  • [ 32991-17-6 ]
  • [ 2900-39-2 ]
  • [ 162457-35-4 ]
  • 2
  • [ 32991-17-6 ]
  • [ 78588-24-6 ]
  • [ 87251-41-0 ]
  • 3
  • [ 32991-17-6 ]
  • (S)-2-(2-Amino-acetylamino)-3-methyl-N-(4-nitro-phenyl)-butyramide; hydrochloride [ No CAS ]
  • [ 87251-42-1 ]
  • 4
  • [ 32991-17-6 ]
  • (S)-3-Methyl-2-(2-methylamino-acetylamino)-N-(4-nitro-phenyl)-butyramide; hydrochloride [ No CAS ]
  • [ 87263-11-4 ]
  • 5
  • [ 32991-17-6 ]
  • H-Pro-Val-pNA hydrochloride [ No CAS ]
  • [ 87251-40-9 ]
  • 6
  • [ 32991-17-6 ]
  • (R)-2-Amino-4-methyl-pentanoic acid [(S)-2-methyl-1-(4-nitro-phenylcarbamoyl)-propyl]-amide; hydrochloride [ No CAS ]
  • [ 87251-43-2 ]
  • 8
  • [ 37783-45-2 ]
  • [ 32991-17-6 ]
  • 10
  • [ 3392-09-4 ]
  • [ 56-40-6 ]
  • [ 32991-17-6 ]
YieldReaction ConditionsOperation in experiment
75.7% With sodium hydrogencarbonate; In 1,4-dioxane; water; REFERENCE EXAMPLE 155 Preparation of Boc-Leu-Gly--OH 2.63 g of H-Gly--OH and 3.50 g of sodium hydrogencarbonate were suspended in 50 ml of water. Thereto was added 50 ml of a dioxane solution containing 10.0 g of Boc-Leu-OSu, and the mixture was stirred for 30 minutes with ice-cooling and then for 15 hours at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was extracted with 70 ml of ethyl acetate. The ethyl acetate layer was washed with 1N hydrochloric acid and a saturated aqueous sodium chloride solution, dried with anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to obtain 6.65 g (yield: 75.7%) of the above objective compound having a melting point of 115-123 C.
  • 11
  • [ 32991-17-6 ]
  • 2-benzyl-3-ethyl-aziridine-2,3-dicarboxylate [ No CAS ]
  • 1-[(2-<i>tert</i>-butoxycarbonylamino-4-methyl-pentanoylamino)-acetyl]-aziridine-2,3-dicarboxylic acid 2-benzyl ester 3-ethyl ester [ No CAS ]
  • 13
  • [ 32991-17-6 ]
  • [ 769111-03-7 ]
  • [ 362626-47-9 ]
  • 15
  • [ 32991-17-6 ]
  • HCl*Leu-Gly-Val-OBzl [ No CAS ]
  • N-(tert-butoxycarbonyl)-leucyl-glycyl-leucyl-glycyl-valine benzyl ester [ No CAS ]
  • 16
  • [ 32991-17-6 ]
  • HCl*H-Leu-Gly-OAll [ No CAS ]
  • [ 362626-47-9 ]
  • 17
  • [ 32991-17-6 ]
  • H-Ala-Gly-OEt*TFA [ No CAS ]
  • [ 406946-00-7 ]
  • 18
  • [ 32991-17-6 ]
  • [ 106644-58-0 ]
  • 19
  • [ 13139-15-6 ]
  • Boc-Arg(Tos)-OHBoc-His(Tos)-OH [ No CAS ]
  • [ 32991-17-6 ]
  • 20
  • [ 32991-17-6 ]
  • [ 406946-01-8 ]
  • 21
  • [ 32991-17-6 ]
  • [ 406946-03-0 ]
  • 22
  • [ 32991-17-6 ]
  • [ 406946-02-9 ]
  • 23
  • [ 32991-17-6 ]
  • H-Leu-Gly-Ala-Gly-Gly-Ala-Gly-OH*TFA [ No CAS ]
  • 24
  • [ 32991-17-6 ]
  • [ 406946-08-5 ]
  • 25
  • [ 32991-17-6 ]
  • [ 406946-07-4 ]
  • 26
  • [ 32991-17-6 ]
  • H-Leu-Gly-Ala-Gly-Gly-Ala-Gly-Val-Leu-OH*TFA [ No CAS ]
  • 30
  • [ 32991-17-6 ]
  • H-Leu-Gly-Leu-Gly-OAll [ No CAS ]
  • 31
  • [ 32991-17-6 ]
  • [ 783296-01-5 ]
  • 33
  • [ 32991-17-6 ]
  • (S)-2-[2-((S)-2-{(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-acetylamino]-3-methyl-butyrylamino}-4-methyl-pentanoylamino)-2-methyl-propionylamino]-3-methyl-butyric acid methyl ester [ No CAS ]
  • 35
  • [ 32991-17-6 ]
  • [ 162457-32-1 ]
 

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