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Chemical Structure| 79032-48-7 Chemical Structure| 79032-48-7
Chemical Structure| 79032-48-7

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Synonyms: S-Nitroso-N-acetylpenicillamine;SNAP

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of D-SNAP

CAS No. :79032-48-7
Formula : C7H12N2O4S
M.W : 220.25
SMILES Code : CC(SN=O)(C)[C@@H](NC(C)=O)C(O)=O
Synonyms :
S-Nitroso-N-acetylpenicillamine;SNAP
English Name :(S)-2-Acetamido-3-methyl-3-(nitrosothio)butanoic acid
MDL No. :MFCD00153852

Safety of D-SNAP

Application In Synthesis of D-SNAP

* 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 [ 79032-48-7 ]

[ 79032-48-7 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 15537-71-0 ]
  • [ 67776-06-1 ]
  • [ 59-53-0 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h;
  • 2
  • [ 15537-71-0 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
72% With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide; trifluoroacetic acid In acetonitrile at 20℃; for 0.5h; Sealed tube;
70% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water for 0.25h;
67% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water at 20℃; for 0.25h;
64% With hydrogenchloride; sulfuric acid; sodium nitrite In methanol; water at 20℃; for 0.5h; 1 Pulverized D-valine, N-acetyl-3-mercapto- (Fluka, 1.91 g, 10 mmol) was suspended in methanol (20 mL). IM HCl (20 mL) and sulfuric acid (2 niL) were added and the reaction mixture was cool to approximately room temperature. Sodium nitrite (1.38 g, 20 mmol) in water (20 mL) was added dropwisely over 5 minutes. D-valine, N-acetyl-3-mercapto- dissolved and formed a green solid. The suspension was stirred at room temperature for 25 minutes. The crystals were collected by filtration and washed with water, dried in vacuum to give the title compound (1.40 g, 64% yield). 1H NMR (300 MHz, CD3OD) δ 5.32 (s, 1 H), 2.04 (s, 3 H), 2.01 (s, 3 H), 1.97 (s, 3 H). . LRMS (APIMS) m/z 221 (MH+), 238 (MNH4+).
With PBS buffer; ethylenediaminetetraacetic acid; S-nitroso bovine serum albumin at 25℃; for 0.166667h;
With sulfuric acid; cis-nitrous acid Cooling with ice;
72 %Spectr. With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide; trifluoroacetic acid In acetonitrile at 20℃; for 0.5h; Sealed tube; [B] General Procedure for Acid Catalyzed Nitrosation. General procedure: The threads of a 3 mL borosilicate scintillation vial were thoroughly taped with Teflon tape. To this vial containing a stir bar was added substrate (0.2 mmol, 1 equiv), and NO-1 (54.0 mg, 0.24 mmol, 1.2 equiv). Acetonitrile (2 mL) and trifluoracetic acid (3.1 pL, 20 mol %) was then added and the reaction was stirred at room temperature until completed (thin-layer chromatography). Upon completion, the solvent was removed under reduced pressure, crude mixture was directly absorbed onto silica and purified by silica gel chromatography to yield the desired product.
78 % With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide In acetonitrile at 80℃;

  • 3
  • [ 59-53-0 ]
  • [ 79032-48-7 ]
  • [ 15537-71-0 ]
  • [ 67776-06-1 ]
YieldReaction ConditionsOperation in experiment
With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h;
  • 4
  • [ 1173106-27-8 ]
  • [ 79032-48-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
In water 2 Hexopyranoside, 4,6-diamino-3-[(3-amino-3-deoxyhexopyranosyl)oxy]-2- hydroxycyclohexyl 2,6-diamino-2,3,6-trideoxy- (SAFC, 31.32 mg, 67.15 mmol) and the product of Example 1 (73.942 mg, 335.72 mmol) were mixed and dissolved in water (5 mL). The resultant solution was freeze dried to give 105 mg of the title compound. NMR (300 MHz, D2O) δ 5.67 (d, J= 3.9 Hz, 1 H), 5.03 (d, J= 3.9 Hz, 1 H), 4.89 (s, 3.75 H), 4.18 (s, 1.25 H), 3.93-3.31 (m, 16 H), 3.18 (dd, J= 7.2 & 13.8 Hz, 1 H), 2.46 (m, 1 H), 2.21 (m 1 H), 2.13-1.71 (m, 2 H), 1.97 (s, 3.4 H), 1.91 (S, 23 H), 1.88 (s, 11.7 H), 1.33 (s, 3.4 H), 1.29 (s, 3.4 H).
  • 5
  • [ CAS Unavailable ]
  • [ 79032-48-7 ]
  • [ 151268-43-8 ]
YieldReaction ConditionsOperation in experiment
In not given (Ar); mixing iron complex with nitroso compd.; not isolated, detected by ESR;
  • 6
  • [ 79032-48-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With 3-(N-morpholino)propanesulfonic acid; ethylenediaminetetraacetic acid; L-Cysteine; potassium chloride; sodium sulfite at 22℃; Electrochemical reaction;
  • 7
  • [ 79032-48-7 ]
  • [ 948836-23-5 ]
YieldReaction ConditionsOperation in experiment
With Cu2O In aq. phosphate buffer at 25℃;
  • 8
  • [ 59-53-0 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; sulfuric acid; sodium nitrite Synthesis of S-Nitroso-N-acetyl-D-penicillamine (SNAP) Equimolar ratios of N-acetylpenicillamine (NAP) and sodium nitrite were added to a reaction vessel, which had 1:1 mixture of water and methanol containing 2 M HCl and 2 M H2SO4, and stirred for 30 minutes. The reaction vessel was cooled in an ice bath to precipitate the SNAP crystals. After precipitation of SNAP crystals, they were collected by filtration and washed with water to remove unreacted salts, and air dried.
  • 9
  • [ 273921-90-7 ]
  • [ 79032-48-7 ]
YieldReaction ConditionsOperation in experiment
Synthesis of S-Nitroso-N-acetyl-D-penicillamine (SNAP) 2 wt % SNAP was dissolved in 80% ethanol and 3 ml of the resulting solution was added into the completely dispersed chitosan and the mixing process was continued to obtain complete encapsulation of SNAP.
  • 10
  • [ 79032-48-7 ]
  • [ 10102-43-9 ]
YieldReaction ConditionsOperation in experiment
With ethylenediaminetetraacetic acid In aq. buffer at 37℃; Darkness;
 

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