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| 93-12-9 Chemical Structure| 93-12-9

Structure of 93-12-9

Chemical Structure| 93-12-9

*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 [ 93-12-9 ]

CAS No. :93-12-9
Formula : C10H12O3S
M.W : 212.27
SMILES Code : O=S(C1=CC=C2CCCCC2=C1)(O)=O
English Name :5,6,7,8-Tetrahydronaphthalene-2-sulfonic acid
MDL No. :MFCD21963037
InChI Key :CTEWUQNEQPLMMJ-UHFFFAOYSA-N
Pubchem ID :67287

Safety of [ 93-12-9 ]

Application In Synthesis of [ 93-12-9 ]

* 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 [ 93-12-9 ]

[ 93-12-9 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 119-64-2 ]
  • [ 93-12-9 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid
With chlorosulfonic acid In chloroform at -10 - 20℃; for 1h; 50 Example 50[00697] Synthesis of 4-((5,6,7,8-tetrahydronaphthalen-2-yl)thio)-lH-l,2,3-triazole-5-carboxylic acid (50) To a solution of Compound 50A (9.66 g, 73 mmol) in CHCb (22 mL) was dropped ClSCbH (26 g, 0.223 mol) at -10 °C. The mixture was stirred at room temperature for 1 hour, poured into ice-water (100 mL), and extracted with dichlorom ethane (100 mL x 2). The combined extracts were dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified with flash column chromatography on silica gel (ethyl acetate in petroleum ether, 10% v/v) to yield Compound 50B. LC-MS (ESI) m/z: non-ionizable compound under routine conditions used. -NMR (CDCb, 400 MHz): d (ppm) 1.83-1.86 (m, 4H), 2.85-2.88 (m, 4H), 7.27-7.29 (m, 1H), 7.71-7.73 (m, 2H).
  • 2
  • [ 119-64-2 ]
  • [ 93-12-9 ]
YieldReaction ConditionsOperation in experiment
durch Sulfurierung;
With chlorosulfonic acid at -10 - -5℃; und Kochen des entstandenen Chloridgemisches mit Wasser;
With chlorosulfonic acid at -10 - -5℃; und Kochen des entstandenen Chloridgemisches mit Wasser;
  • 3
  • [ 93-12-9 ]
  • [ 1730-48-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: durch Kalischmelze 2: alkali
Multi-step reaction with 2 steps 1: durch Kalischmelze 2: im Autoklaven
Multi-step reaction with 2 steps 1: durch Kalischmelze 2: NaOH-solution
  • 4
  • [ 93-12-9 ]
  • [ 854912-52-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: durch Kalischmelze 2: carbon tetrachloride; bromine 3: sulfuric acid
Multi-step reaction with 3 steps 1: durch Kalischmelze 2: sulfuric acid 3: bromine
  • 5
  • [ 93-12-9 ]
  • [ 24634-91-1 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; zinc In ethanol at 80℃; for 1.5h; 50 To a mixture of Compound 50B (1.5 g, 6.5 mmol) and Zn powder (2.5 g, 38.2 mmol) in ethanol (10 mL) was dropped concentrated HC1 (10 mL) over a period of 30 minutes. After the mixture was stirred at 80 °C for 1 hour and cooled down to room temperature, it was filtered. The filtration was diluted with ethyl acetate (200 mL). The organic phase was washed with brine (200 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to yield Compound 50C. LC-MS (ESI) m/z: 163 [M-H]; ‘H-NIVIR (CDC13, 400 MHz): (5(ppm) 1.75- 1.78 (m, 4H), 2.68-2.72 (m, 4H), 3.34 (s, 1H), 6.92-6.94 (m, 1H), 7.00-7.02 (m, 2H).
  • 6
  • [ 93-12-9 ]
  • [ 2361219-68-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: hydrogenchloride; zinc / ethanol / 1.5 h / 80 °C 2: N,N-dimethyl-formamide / 16 h / 50 °C
  • 7
  • [ 93-12-9 ]
  • [ 1368960-74-0 ]
YieldReaction ConditionsOperation in experiment
27% With potassium 2-(difluoro(trifluoromethoxy)methoxy)-2,2-difluoroacetate In N,N-dimethyl-formamide at 135℃; for 2h; Schlenk technique; Sealed tube; Glovebox; Inert atmosphere;
 

Historical Records

Technical Information

Categories