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| 175205-49-9 Chemical Structure| 175205-49-9

Structure of 175205-49-9

Chemical Structure| 175205-49-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

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 [ 175205-49-9 ]

CAS No. :175205-49-9
Formula : C9H9N3S
M.W : 191.25
SMILES Code : NCC1=CC=C(C2=CSN=N2)C=C1
English Name :(4-(1,2,3-Thiadiazol-4-yl)phenyl)methanamine
MDL No. :MFCD02682075

Safety of [ 175205-49-9 ]

Application In Synthesis of [ 175205-49-9 ]

* 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 [ 175205-49-9 ]

[ 175205-49-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 17641-39-3 ]
  • [ 175205-49-9 ]
  • [ 1357470-42-8 ]
YieldReaction ConditionsOperation in experiment
80% With N-ethyl-N,N-diisopropylamine In dichloromethane at 25℃; for 5h; General Procedure for synthesis of compounds 4 General procedure; To a stirred of compound 3 (1.0 eq) and thiadiazolylbenzyl amine (1.0 eq) in dry DCM was added DIEA (1.1 eq) at 25 oC. The reaction mixture was stirred at 25 oC for 5 hrs. The reaction mixture was diluted with DCM, washed with water followed by brine solution, dried over sodium sulfate and concentrated to afford a solid product. Chromatography (100-200 mesh size silica gel column, 0-30% ethyl acetate: hexane) afforded the title compound. Off White solid; Yield: 80%; mp: 93-94C; 1H NMR (400 MHz, Acetone-d6): δ = 4.37 (s, 2H), 4.94 (s, 2H), 7.01-7.15 (m, 4H), 7.32-7.36 (m, 2H), 7.79-7.85 (m, 2H), 8.21 (s, 1H), 11.1 (s, 1H); 13C NMR (100 MHz, Acetone-d6): δ 46.4, 67.8, 113.2, 114.8, 127.5, 127.8, 128.1, 128.4, 130.1, 131.2, 132.1, 141.8, 161.7, 163.3, 173.0; ESI/MS m/z: 406.4 (M+1); Calcd/Anal. for C17H15N3O5S2: [C (50.36) 50.38; H (3.73) 3.71; N 10.36) 10.35].
With N-ethyl-N,N-diisopropylamine In dichloromethane
  • 2
  • [ 17641-39-3 ]
  • [ 175205-49-9 ]
  • [ 863977-54-2 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine In dichloromethane at 25℃; for 5h; General Procedure for synthesis of compounds 4 General procedure; To a stirred of compound 3 (1.0 eq) and thiadiazolylbenzyl amine (1.0 eq) in dry DCM was added DIEA (1.1 eq) at 25 oC. The reaction mixture was stirred at 25 oC for 5 hrs. The reaction mixture was diluted with DCM, washed with water followed by brine solution, dried over sodium sulfate and concentrated to afford a solid product. Chromatography (100-200 mesh size silica gel column, 0-30% ethyl acetate: hexane) afforded the title compound. Off White solid; Yield: 80%; mp: 93-94C; 1H NMR (400 MHz, Acetone-d6): δ = 4.37 (s, 2H), 4.94 (s, 2H), 7.01-7.15 (m, 4H), 7.32-7.36 (m, 2H), 7.79-7.85 (m, 2H), 8.21 (s, 1H), 11.1 (s, 1H); 13C NMR (100 MHz, Acetone-d6): δ 46.4, 67.8, 113.2, 114.8, 127.5, 127.8, 128.1, 128.4, 130.1, 131.2, 132.1, 141.8, 161.7, 163.3, 173.0; ESI/MS m/z: 406.4 (M+1); Calcd/Anal. for C17H15N3O5S2: [C (50.36) 50.38; H (3.73) 3.71; N 10.36) 10.35].
 

Historical Records

Technical Information

Categories