Home Cart Sign in  
Chemical Structure| 42590-97-6 Chemical Structure| 42590-97-6

Structure of 42590-97-6

Chemical Structure| 42590-97-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

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

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

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

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

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

Alternative Products

Product Details of [ 42590-97-6 ]

CAS No. :42590-97-6
Formula : C8H9NOS
M.W : 167.23
SMILES Code : NC(C1=CC=CC=C1OC)=S
MDL No. :MFCD04973324

Safety of [ 42590-97-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 42590-97-6 ]

* 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 [ 42590-97-6 ]

[ 42590-97-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6609-56-9 ]
  • [ 42590-97-6 ]
YieldReaction ConditionsOperation in experiment
89% With pyridine; diammonium sulfide; triethylamine; In water; at 0 - 55℃; To a stirred solution of 2-methoxy benzo nitrile (130 g, 977 mmol) in pyridine (1200 mL) at 0oC was added ammonium sulfide solution (650 mL, 5 vol), followed by triethyl amine (150 mL, 1075 mmol). Then the reaction mixture was stirred at 55 oC for 12h. The reaction was monitored by TLC (30 % Ethyl acetate/Hexane). After completion of the reaction, diluted with cold water (4.0 L), solid was filtered, dried over vacuum to afford 2- methoxybenzothioamide (145 g, yield: 89%) as a yellow solid.1H NMR (400 MHz, DMSO- d6) δ 9.94 br(s, 1H), 9.30 (brs, 1H), 7.68 (d, J = 7.6 Hz, 1H), 7.36 (t, J = 8.0 Hz, 1H), 7.04 (d, J = 8.4 Hz, 1H), 6.94 (t, J = 7.2 Hz, 1H), 3.79 (s, 3H).
 

Historical Records

Technical Information

Categories