Home Cart Sign in  
Chemical Structure| 1186518-98-8 Chemical Structure| 1186518-98-8

Structure of 1186518-98-8

Chemical Structure| 1186518-98-8

*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 [ 1186518-98-8 ]

CAS No. :1186518-98-8
Formula : C8H7BrO4S
M.W : 279.11
SMILES Code : O=C(O)C1=CC(S(=O)(C)=O)=CC(Br)=C1
MDL No. :MFCD24107191

Safety of [ 1186518-98-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1186518-98-8 ]

* 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 [ 1186518-98-8 ]

[ 1186518-98-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56622-54-9 ]
  • [ 1186518-98-8 ]
  • [ 1186518-99-9 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; To a mixture of 3-bromo-5-(methylsulfonyl)benzoic acid (630 mg, 2.2 mmol), N-(3- dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (860 mg, 4.5 mmol), 1 -hydroxybenzotriazole hydrate (140 mg, 0.90 mmol), and CH2Cl2 (25 mL) were added <strong>[56622-54-9](6-methylpyridin-3-yl)methanamine</strong> (550 mg, 4.5 mmol) and NN-diisopropylethylamine (0.79 mL, 4.5 mmol). The mixture was stirred at room temperature overnight, and then diluted with CH2Cl2 (50 mL). The organic phase was washed with water and aq. Na2CO3 solution, dried (Na2SO4), and concentrated in vacuo. The residue was purified by silica gel column (50-100% EtOAc/hexane) to afford a white solid. LC-MS: 385.2 [M+l]+; 1H NMR (400 MHz, CDCl3): 8.51 (d, IH, J = 1.6 Hz), 8.28 (t, IH, J = 1.6 Hz), 8.23 (t, IH, J = 1.6 Hz), 8.19 (t, IH, J = 1.6 Hz), 7.66 (dd, IH, J = 8.0, 2.0 Hz), 7.19 (d, IH, J = 8.0 Hz), 6.93 (bs, IH), 4.63 (d, 2H, J = 5.6 Hz), 3.09 (s, 3H), 2.57 (s, 3H).
 

Historical Records

Technical Information

Categories