Home Cart Sign in  
Chemical Structure| 207923-07-7 Chemical Structure| 207923-07-7

Structure of 207923-07-7

Chemical Structure| 207923-07-7

*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 [ 207923-07-7 ]

CAS No. :207923-07-7
Formula : C8H11NO
M.W : 137.18
SMILES Code : CCC1=CC=C(C=C1O)N

Safety of [ 207923-07-7 ]

Application In Synthesis of [ 207923-07-7 ]

* 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 [ 207923-07-7 ]

[ 207923-07-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 20191-74-6 ]
  • [ 207923-07-7 ]
  • 2
  • [ 207923-07-7 ]
  • [ 101537-64-8 ]
  • 3-tert-butyloxycarbonylamino-N-(4-ethyl-3-hydroxyphenyl)thiophen-2-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
60% With triethylamine; HATU; In N,N-dimethyl-formamide; for 18h; The mixture of 5-amino-2-ethylphenol (500 mg, 3.65 mmol), N- i-butyloxycarbonyl 3-aminothiophene-2- carboxylic acid (931 mg, 3.83 mmol), (l-[bis(dimethylamino)methylene]-lH-l ,2,3-triazolo[4,5- bjpyridinium 3-oxid hexafluorophosphate) (1.8 g, 4.75 mmol), Et3N (2.0 mL) in dimethylformamide (20 mL) was stirred for 18 hours. The mixture was poured into water (250 mL), extracted by ethyl acetate (3x50 mL). The combined extracts were washed with brine (50 mL), dried and concentrated. The residue was purified by flash column (40g) to give i-butyloxycarbonyl protected intermediate (773 mg, 60%). LC/MS: RT = 5.78 minutes, purity > 95%, (M-100+H)+ = 262.96.
  • 3
  • [ 52427-05-1 ]
  • [ 207923-07-7 ]
 

Historical Records