Home Cart Sign in  
Chemical Structure| 4783-83-9 Chemical Structure| 4783-83-9

Structure of 4783-83-9

Chemical Structure| 4783-83-9

*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 [ 4783-83-9 ]

CAS No. :4783-83-9
Formula : C11H8N2O3
M.W : 216.19
SMILES Code : O=[N+](C1=CC=C(OC2=CC=NC=C2)C=C1)[O-]
MDL No. :MFCD07778622
InChI Key :WNLPFSUCTGPURU-UHFFFAOYSA-N
Pubchem ID :44558538

Safety of [ 4783-83-9 ]

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

Application In Synthesis of [ 4783-83-9 ]

* 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 [ 4783-83-9 ]

[ 4783-83-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4783-83-9 ]
  • [ 102877-78-1 ]
YieldReaction ConditionsOperation in experiment
76% With hydrogen;palladium on activated charcoal; In methanol; at 20℃; b) Compound 1 was hydrogenated at room temperature using Pd/C in MESH. The reaction solution was filtered through kieselguhr and rinsed with MEOH, and the filtrate was subsequently evaporated. The residue was digested with diethyl ether : petroleum ether = 2 : 1, filtered off with suction, rinsed with petroleum ether and dried overnight at 40C under reduced pressure. Yield : 50. 94 G (76%) of 2, brown crystals
76% With hydrogen;palladium on activated charcoal; In methanol; at 20℃; The thus obtained nitro comound was hydrogenated at room temperature using Pd/C in MEOH. The reaction solution was filtered through kieselguhr and rinsed with MEOH, and the filtrate was subse- quently evaporated. The residue was digested with diethyl ether : petroleum ether = 2: 1, filtered off with suction, rinsed with petroleum ether and dried overnight at 40C under reduced pressure. Yield : 50.94 g (76%) of 5a, brown crystals
76% With hydrogen;palladium on activated charcoal; In methanol; Compound 1 is hydrogenated with Pd/C in methanol. The reaction mixture is filtered over kieselguhr, the residue washed with methanol and the filtrate evaporated. The residue is digested with a diethyl ether/petroleum ether-mixture (2: 1), filtered by suction, washed with petrol ether and dried in vaccuo at 40 [C] overnight to yield 50.94 g (76 %) brownish crystals of 2.
76% With hydrogen;palladium on activated charcoal; In methanol; at 20℃; b) Compound 1 was hydrogenated using Pd/C in MeOH at room temperature. The reaction solution was filtered through kieselguhr, the filter cake was rinsed with MeOH, and the filtrate was subsequently evaporated. The residue was digested with diethyl ether : petroleum ether = 2: 1, filtered off with suction, rinsed with petroleum ether and dried at 40C under reduced pressure overnight. Yield : 50.94 g (76%) of 2, brown crystals
76% With hydrogen;palladium on activated charcoal; In methanol; at 20℃; b) Compound 1 is hydrogenated at room temperature using Pd/C in MeOH. The reaction solution is filtered through kieselguhr and rinsed with MeOH, and the filtrate is subsequently evaporated. The residue is digested with diethyl ether: petroleum ether = 2: 1, filtered off with suction, rinsed with petroleum ether and dried overnight at 40C under reduced pressure. Yield : 50.94 g (76%) of 2, brown crystals
76% With hydrogen;palladium on activated charcoal; at 20℃; b) The thus obtained nitro-compound is hydrogenated using Pd/C in MeOH at room temperature. The reaction mixture is filtered and the filtrate is evaporated. The residue is digested with diethyl ether: petroleum ether = 2: 1, filtered by suction, rinsed with petroleum ether and dried in vacuo Yield : 50.94 g (76 %) 24, brown crystals

 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 4783-83-9 ]

Aryls

Chemical Structure| 28232-53-3

A756450 [28232-53-3]

3-(4-Nitrophenoxy)pyridine

Similarity: 0.92

Chemical Structure| 208122-66-1

A342378 [208122-66-1]

3-Nitro-5-(pyridin-3-yloxy)aniline

Similarity: 0.88

Chemical Structure| 32841-11-5

A349617 [32841-11-5]

3-Nitro-9-phenoxyacridine

Similarity: 0.87

Chemical Structure| 190728-24-6

A443694 [190728-24-6]

6,7-Dimethoxy-4-(4-nitrophenoxy)quinoline

Similarity: 0.85

Chemical Structure| 57580-69-5

A808835 [57580-69-5]

1-Nitro-8-phenoxyacridine

Similarity: 0.85

Ethers

Chemical Structure| 28232-53-3

A756450 [28232-53-3]

3-(4-Nitrophenoxy)pyridine

Similarity: 0.92

Chemical Structure| 208122-66-1

A342378 [208122-66-1]

3-Nitro-5-(pyridin-3-yloxy)aniline

Similarity: 0.88

Chemical Structure| 32841-11-5

A349617 [32841-11-5]

3-Nitro-9-phenoxyacridine

Similarity: 0.87

Chemical Structure| 874498-45-0

A836140 [874498-45-0]

4-Methoxy-6-nitroquinoline

Similarity: 0.87

Chemical Structure| 190728-24-6

A443694 [190728-24-6]

6,7-Dimethoxy-4-(4-nitrophenoxy)quinoline

Similarity: 0.85

Nitroes

Chemical Structure| 28232-53-3

A756450 [28232-53-3]

3-(4-Nitrophenoxy)pyridine

Similarity: 0.92

Chemical Structure| 208122-66-1

A342378 [208122-66-1]

3-Nitro-5-(pyridin-3-yloxy)aniline

Similarity: 0.88

Chemical Structure| 32841-11-5

A349617 [32841-11-5]

3-Nitro-9-phenoxyacridine

Similarity: 0.87

Chemical Structure| 874498-45-0

A836140 [874498-45-0]

4-Methoxy-6-nitroquinoline

Similarity: 0.87

Chemical Structure| 57580-69-5

A808835 [57580-69-5]

1-Nitro-8-phenoxyacridine

Similarity: 0.85

Related Parent Nucleus of
[ 4783-83-9 ]

Pyridines

Chemical Structure| 28232-53-3

A756450 [28232-53-3]

3-(4-Nitrophenoxy)pyridine

Similarity: 0.92

Chemical Structure| 208122-66-1

A342378 [208122-66-1]

3-Nitro-5-(pyridin-3-yloxy)aniline

Similarity: 0.88