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


  • CasNo 51871-62-6
  • Purity 99%
Inquery

Quality Factory Supply 99% Pure (S)-3-(Boc-amino)-4-phenylbutyric acid 51871-62-6 with Efficient Delivery

  • Molecular Formula: C15H21 N O4
  • Molecular Weight: 279.336
  • Melting Point: 100-104 ºC 
  • Boiling Point: 444.8°Cat760mmHg 
  • PKA: 4.43±0.10(Predicted) 
  • Flash Point: 222.8°C 
  • PSA: 75.63000 
  • Density: 1.139 
  • LogP: 2.98800 

51871-62-6 Relevant articles

Synthesis of enantiomerically pure δ-benzylproline derivatives

Rodríguez, Isabel,Calaza, M. Isabel,Jiménez, Ana I.,Cativiela, Carlos

, p. 3310 - 3318 (2015)

The (2S,5R) stereoisomer of 5-benzylprol...

Synthesis method of chiral N-Boc-3-amino-4-aryl-butyric acid

-

Paragraph 0032; 0033; 0034; 0035; 0036, (2017/08/28)

The invention relates to a synthesis met...

Protein-protein interface mimicry by an oxazoline piperidine-2,4-dione

Li, Xun,Taechalertpaisarn, Jaru,Xin, Dongyue,Burgess, Kevin

supporting information, p. 632 - 635 (2015/03/05)

Representative minimalist mimics 1 were ...

Antiplasmodial activity of new 4-aminoquinoline derivatives against chloroquine resistant strain

Sinha, Manish,Dola, Vasanth R.,Agarwal, Pooja,Srivastava, Kumkum,Haq, Wahajul,Puri, Sunil K.,Katti, Seturam B.

, p. 3573 - 3586 (2014/07/07)

Emergence and spread of multidrug resist...

51871-62-6 Process route

(3S)-tert-butyl 1-benzyl-3-diazo-2-oxopropylcarbamate
60398-41-6

(3S)-tert-butyl 1-benzyl-3-diazo-2-oxopropylcarbamate

(S)-3-tert-butoxycarbonylamino-4-phenylbutanoic acid
51871-62-6

(S)-3-tert-butoxycarbonylamino-4-phenylbutanoic acid

Conditions
Conditions Yield
With silver benzoate; In 1,4-dioxane; water; microwave irradiation;
90%
With silver benzoate; sodium carbonate; In 1,4-dioxane; water; at 20 ℃; for 0.75h; Sonication;
86%
With silver benzoate; In 1,4-dioxane; water; at 70 ℃;
82%
With water; silver(I) acetate; triethylamine; In tetrahydrofuran; for 3h;
76%
With silver trifluoroacetate; In tetrahydrofuran; water; triethylamine; at 20 ℃; for 3h;
44%
With hydrogenchloride; sodium carbonate; sodium thiosulfate; silver(l) oxide; Yield given. Multistep reaction; 1.) water, dioxane, 81-85 deg C, 1.5 h 2.) water, 5 deg C;
With sodium carbonate; sodium thiosulfate; silver(l) oxide; In 1,4-dioxane; water; for 1h; Heating;
With silver benzoate; In 1,4-dioxane; water; at 70 ℃; for 5h;
With silver trifluoroacetate;
With TEA; silver trifluoroacetate; In tetrahydrofuran; at 20 ℃; for 4h;
Multi-step reaction with 2 steps
1: 70 percent / silver benzoate; Et3 N / tetrahydrofuran / 3 h / 20 °C
2: H2 / Pd/C / methanol / 10 h / 750.06 Torr
With hydrogen; silver benzoate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol;
Multi-step reaction with 2 steps
1: 100 percent / silver benzoate; Et3 N / 18 h / 20 °C
2: 19 percent / 10 percent aq. NaOH / methanol / 18 h / 20 °C
With sodium hydroxide; silver benzoate; triethylamine; In methanol; 1: Rearrangement / 2: Hydrolysis;
With silver benzoate; silica gel; In ethyl acetate; at 50 ℃; for 0.5h;
(3S)-tert-butyl 1-benzyl-3-diazo-2-oxopropylcarbamate; In tetrahydrofuran; at 20 ℃; for 0.166667h; Irradiation; Flow reactor;
With water; Flow reactor;
methyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate
60398-42-7,142854-48-6

methyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate

(S)-3-tert-butoxycarbonylamino-4-phenylbutanoic acid
51871-62-6

(S)-3-tert-butoxycarbonylamino-4-phenylbutanoic acid

Conditions
Conditions Yield
With lithium hydroxide; water; In 1,4-dioxane; for 20h;
92%
With sodium hydroxide; In methanol; at 20 ℃; for 18h;
19%
With potassium carbonate; In methanol; water;
With lithium hydroxide; In 1,4-dioxane; water; for 20h;
With lithium hydroxide; In tetrahydrofuran; methanol; water;
With water; sodium hydroxide; In methanol; at 0 - 20 ℃; for 2h;

51871-62-6 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 13734-34-4
    13734-34-4

    N -tert -butoxycarbonyl-L -phenylalanine

  • 60398-41-6
    60398-41-6

    (3S)-tert-butyl 1-benzyl-3-diazo-2-oxopropylcarbamate

  • 60398-42-7
    60398-42-7

    methyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate

51871-62-6 Downstream products

  • 115364-92-6
    115364-92-6

    (S)-N-tert-butyloxycarbonyl-3-amino-4-phenyl-N'-(benzyloxy)butanamide

  • 130944-47-7
    130944-47-7

    3-[(tert-butoxycarbonyl)amino]-4-phenylbutanaldehyde

  • 114645-20-4
    114645-20-4

    (S)-3-amino-4-phenylbutanoic acid trifluoroacetate

  • 138165-77-2
    138165-77-2

    (S)-3-amino-4-phenylbutanoic acid hydrochloride

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