Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 1956318-90-3 Chemical Structure| 1956318-90-3
Chemical Structure| 1956318-90-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

2-Methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate is a bis-sulfone-PNP linker for antibody-drug-conjugation (ADC).

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

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of PDdEC-NB

CAS No. :1956318-90-3
Formula : C16H16N2O5S2
M.W : 380.43
SMILES Code : O=C(OCC(SSC1=NC=CC=C1)(C)C)OC2=CC=C([N+]([O-])=O)C=C2
English Name :2-Methyl-2-(pyridin-2-yldisulfaneyl)propyl (4-nitrophenyl) carbonate
MDL No. :MFCD28556917

Safety of PDdEC-NB

Application In Synthesis of PDdEC-NB

* 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 [ 1956318-90-3 ]

[ 1956318-90-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5070-13-3 ]
  • [ 3034751-98-6 ]
  • [ 1956318-90-3 ]
YieldReaction ConditionsOperation in experiment
1.4 g With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; for 7h; 14 General procedure for preparation of compound 4 To a solution of compound 3 (5.67 g, 26.3 mrnol, 1.00 eq.) in DMF (25.0 mL) was added DIEA(10.2 g, 78.9 mmol, 13.7 rnL, 3.00 eq.) and PNP (16.0 g, 52.6 mmol, 2.00 eq.). The mixture was stirred at 25 °C for 7 hrs. LCMS showed compound 3 was consumed completely and desired mass (MS cal.:380.05, MS observed: [M+Hj = 381.0) was detected. The reaction mixture was diluted with H20 (100 mL) and extracted with EtOAc (50 mL * 3). The combined organic layers were washed with brine (50 mL * 3), dried over Na2SO4, filtered and concentrated under reduced pressure to give a residue. Theresidue was purified by prep-HPLC (0.1% TFA condition) to give compound 4(1.40 g, 3.66 mmol, 3 1.8% yield for 2 steps, 99.4% purity) as a yellow solid which was confirmed via LCMS, HPLC and 1H NMR. LCMS: R = 0.48 mm, MS cal.: 380.0, MS observed: [M+H]+ = 381.1. HPLC: R= 3.53 min, purity: 99.4%. 1H NMR (400 MHz, CDC13) : 8.47 - 8.45 (m, 1H), 8.30 - 8.26 (m, 2H), 7.76 - 7.74 (m, 1H),7.65 -7.60 (m, 2H), 7.39 -7.35 (m, 2H), 7.11 - 7.07 (m, 1H).
1.4 g With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; for 7h; 24 Procedure for preparation of compound 4 To a solution of compound 3 (5.67 g, 26.3 mmol, 1.00 eq.) in DMF (25.0 mL) was added DIEA (10.2 g, 78.9 mmol, 13.7 mL, 3.00 eq.) and PNP (16.0 g, 52.6 mmol, 2.00 eq.). The mixture was stirred at 25 °C for 7 hrs. LCMS showed compound 3 was consumed completely and desired mass (MS cal.: 380.05, MS observed: [M+H]+ = 381.0) was detected. The reaction mixture was diluted with H2O (100 mL) and extracted with EtOAc (50 mL * 3). The combined organic layers were washed with brine (50 mL * 3), dried over Na2SO4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (0.1% TFA condition) to give compound 4 (1.40 g, 3.66 mmol, 31.8% yield for 2 steps, 99.4% purity) as a yellow solid which was confirmed via LCMS, HPLC and HNMR. LCMS: Rt = 0.48 min, MS cal.: 380.0, MS observed: [M+H]+ = 381.1. HPLC: Rt = 3.53 min, purity: 99.4%.1H NMR: 400 MHz, CDCl3 δ: 8.47 - 8.45 (m, 1H), 8.30 - 8.26 (m, 2H), 7.76 - 7.74 (m, 1H), 7.65 - 7.60 (m, 2H), 7.39 - 7.35 (m, 2H), 7.11 - 7.07 (m , 1H).
  • 2
  • [ 2127-03-9 ]
  • [ 1956318-90-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: acetic acid / ethanol / 16 h / 25 °C 2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 7 h / 25 °C
Multi-step reaction with 2 steps 1: acetic acid / ethanol / 16 h / 25 °C 2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 7 h / 25 °C
 

Historical Records

Categories