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Chemical Structure| 51871-62-6 Chemical Structure| 51871-62-6
Chemical Structure| 51871-62-6

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Boc-β-HoPhe-OH is a protected β-hydroxyphenylalanine derivative with the amino group protected by tert-butoxycarbonyl (Boc), suitable for peptide synthesis.

Synonyms: (S)-3-(Boc-amino)-4-phenylbutyric acid

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Product Details of Boc-β-HoPhe-OH

CAS No. :51871-62-6
Formula : C15H21NO4
M.W : 279.33
SMILES Code : O=C(O)C[C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1
Synonyms :
(S)-3-(Boc-amino)-4-phenylbutyric acid
MDL No. :MFCD01076271
InChI Key :ACKWQHCPHJQANL-LBPRGKRZSA-N
Pubchem ID :2761538

Safety of Boc-β-HoPhe-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of Boc-β-HoPhe-OH

* 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 [ 51871-62-6 ]

[ 51871-62-6 ] Synthesis Path-Downstream   1~2

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  • 2
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  • [ 15099-85-1 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In dichloromethane; at 20℃; for 2h; [00293] (S)-3-Amino-4-phenylbutanoic acid: (S)-3-(tert-Butoxycarbonyl)-4- phenylbutanoic acid (Ig, 3.58 mmol) was dissolved in 20 mL DCM and 6 mL TFA was added at room temperature. The mixture was stirred for 2 hours and the mixture was azeotroped 3 times with 25 mL toluene (each). The product thus obtained was used without further purification in the next step. LCMS (API-ES) m/z (%): 179.1 (100%, M++H).
 

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