Home Cart Sign in  
Chemical Structure| 165667-51-6 Chemical Structure| 165667-51-6

Structure of 165667-51-6

Chemical Structure| 165667-51-6

*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 [ 165667-51-6 ]

CAS No. :165667-51-6
Formula : C10H16N2O3S
M.W : 244.31
SMILES Code : O=C(OC(C)(C)C)NCC1=NC(CO)=CS1
MDL No. :MFCD20924985

Safety of [ 165667-51-6 ]

Application In Synthesis of [ 165667-51-6 ]

* 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 [ 165667-51-6 ]

[ 165667-51-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 96929-05-4 ]
  • [ 165667-51-6 ]
YieldReaction ConditionsOperation in experiment
92% With methanol; lithium borohydride; In diethyl ether; for 16h;Heating / reflux; To compound 388 (4.70 g, 16.4 mmol) dissolved in EtzO (140 mL) was added lithium borohydride (1.43 g, 65.7 mmol) and MeOH (2.10 g, 2.7 mL, 65.7 mmol). Refluxed for 16 h, cooled to room temperature, and concentrated. Added water (100 mL), extracted with CH2Cl2, dried combined organic extracts (MgS04), filtered, and concentrated. Purified by silica gel chromatography (eluant: 2% MeOH-CH2C12 to 5% MeOH-CH2CI2) to give 3.70 g (92%) of the product 389 as a yellow solid. MS m/e: 245 (M+H). For n=2: MS m/e: 259 (M+H)
59% With lithium aluminium tetrahydride; In Petroleum ether; a. Tert-butyl N-[[4-(hydroxymethyl)thiazol-2-yl]methyl]carbamate To a stirred solution of <strong>[96929-05-4]ethyl 2-(((tert-butoxycarbonyl)amino)methyl)thiazole-4-carboxylate</strong> (1 g, 3.49 mmol) in THF (20 mL) was added LiAlH4 (7.0 mL, 6.98 mmol, 1M in THF) drop wise under nitrogen at 0 C and the reaction mixture was allowed stir at room temperature for 4 h. The reaction mixture was cooled to 0 C and quenched with EtOAc (30 mL) followed by saturated aqueous sodium sulphate solution. Then stirred at same temperature for 30 min., filtered and filtrate was evaporated. The crude was chromatographed on silica eluting with 40% EtOAc in petroleum ether affording a yellow solid (510 mg, 59%). M/z 245.1 (M+H)+.
  • 2
  • [ 89226-13-1 ]
  • [ 165667-51-6 ]
 

Historical Records