Home Cart Sign in  
Chemical Structure| 214337-39-0 Chemical Structure| 214337-39-0

Structure of 214337-39-0

Chemical Structure| 214337-39-0

*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 [ 214337-39-0 ]

CAS No. :214337-39-0
Formula : C8H6BrNOS
M.W : 244.11
SMILES Code : COC1=CC2=C(SC(Br)=N2)C=C1
MDL No. :MFCD09749263

Safety of [ 214337-39-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 214337-39-0 ]

* 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 [ 214337-39-0 ]

[ 214337-39-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 55690-60-3 ]
  • [ 214337-39-0 ]
YieldReaction ConditionsOperation in experiment
With bromine; In chloroform; at 0℃; for 1.5h; Step 1.Synthesis of 2-bromo-5-methoxybenzothiazole A solution of bromine (3.6 eq) in chloroform (0.75M) was added dropwise over a period of 1 hr to a stirred suspension of <strong>[55690-60-3]5-methoxy-2-mercaptobenzothiazole</strong> (1 eq) in chloroform at 0 C. The mixture was stirred for 30 min before it was added slowly to water and stirred for further 20 min.The mixture was filtered to remove a cream solid.The organic phase was dried and evaporated to leave a brown solid.The brown solid was dissolved in ether and filtered.The residue was washed with ether and the filtrate and washings were combined and evaporated, chromatographed (4:1 hexanes and ethyl acetate) to give the title compound as a pale yellow solid. MS: MH+=244
With bromine; In dichloromethane; chloroform; at 0 - 20℃; A solution of bromine (1.2g, 7.5mmol) was added drop wise over a period of 1h to a stirred suspension of <strong>[55690-60-3]5-methoxy-2-mercaptobenzothiazole</strong> (1g, 5mmol) (7) in chloroform at 0oC. The mixture was stirred for 0.5h before it was added slowly to water and stirred for another 0.5h. The mixture was filtered to remove a creamy solid. The organic phase was dried with sodium sulfate and evaporated to obtain a brown solid. The brown solid was dissolved in ether and filtered. The residue was washed with ether and the filtrate and washings were combined and concentrated and chromatographed using 4:1 hexanes and ethyl acetate as the eluting solvent to give the title compound as a pale yellow solid. m/z: 242/244 (MH+).
  • 2
  • [ 5369-19-7 ]
  • [ 214337-39-0 ]
  • [ 1312543-47-7 ]
YieldReaction ConditionsOperation in experiment
1.01 g With N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; at 220℃;Microwave irradiation; The mixture containing 2-bromo-5-methoxybezothiazole (1g, 4.1mmol) (8), 3-tert-butyl aniline (1.23g, 8.2mmol) and diisopropylethylamine (1.06g, 8.2mmol) was subjected to the microwave in N-methylpyrrolidinone at 220 oC. The resultant mixture was concentrated and partitioned between ethylacetate and water. The organic layer was washed with brine and dried with sodium sulfate. It was then chromatographed on silica gel and eluted with ethyl acetate and hexane to give the 1.01g of N-(3-tert-butylphenyl)-5-methoxybenzo[d]thiazol-2-amine. m/z: 313 (MH+).
 

Historical Records

Technical Information

Categories