Home Cart Sign in  
Chemical Structure| 354525-36-3 Chemical Structure| 354525-36-3

Structure of 354525-36-3

Chemical Structure| 354525-36-3

*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 [ 354525-36-3 ]

CAS No. :354525-36-3
Formula : C8H9NO4
M.W : 183.16
SMILES Code : OCC1=CC([N+]([O-])=O)=CC(OC)=C1
MDL No. :MFCD11870182
InChI Key :YHVWSNFJLXOVCZ-UHFFFAOYSA-N
Pubchem ID :45091344

Safety of [ 354525-36-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 354525-36-3 ]

* 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.

  • Upstream synthesis route of [ 354525-36-3 ]

[ 354525-36-3 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 354525-36-3 ]
  • [ 354512-22-4 ]
YieldReaction ConditionsOperation in experiment
76% With dipyridinium dichromate In dichloromethane at 10 - 20℃; for 3 h; [0095] Step 3. To a solution of (3-methoxy-5-nitrophenyl)methanol (75 g, 0.41 mol) in CH2C12 (1.5 L) was added pyridinium dichromate (382 g, 1.02 mol) and silica gel (382 g) below 10 °C. After stirring at room temperature for 3 h, TLC analysis showed the starting material was consumed completely (3: 1 petroleum/ethyl acetate, Rf 0.6). The mixture was purified by flash column chromatography using CH2C12 to afford 3-methoxy-5-nitrobenzaldehyde as a yellow solid (170 g, 76percent, 3 batches).
References: [1] Patent: WO2013/148365, 2013, A1, . Location in patent: Paragraph 0095.
[2] Journal of Medicinal Chemistry, 2004, vol. 47, # 11, p. 2897 - 2905.
[3] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304.
 

Historical Records

Technical Information

Categories