Home Cart Sign in  
Chemical Structure| 80379-10-8 Chemical Structure| 80379-10-8

Structure of 80379-10-8

Chemical Structure| 80379-10-8

*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 [ 80379-10-8 ]

CAS No. :80379-10-8
Formula : C8H9NO3
M.W : 167.16
SMILES Code : C[C@@H](C1=CC=CC=C1[N+]([O-])=O)O
MDL No. :MFCD18339563

Safety of [ 80379-10-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 80379-10-8 ]

* 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 [ 80379-10-8 ]

[ 80379-10-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 88-72-2 ]
  • [ 68-12-2 ]
  • [ 15121-84-3 ]
  • [ 80379-10-8 ]
YieldReaction ConditionsOperation in experiment
72% With potassium hydroxide; paraformaldehyde; In water; EXAMPLE 1 A mixture of 137 g (1 mole) of o-nitrotoluene, 60 g of paraformaldehyde and 400 ml of dimethyl formamide containing 0.5percent by weight of water is heated to 70° C. under stirring. Thereafter 40 g of potassium hydroxide, covered with 100 ml dimethyl formamide, are added to the mixture at such a rate that the temperature of the reaction mixture does not increase above 120° C. The resulting mixture is stirred for 3 minutes at a temperature above 85° C., thereafter it is cooled and filtered through a sintered glass filter. The filtrate is acidified with hydrochloric acid to pH=3, filtered again, and the resulting filtrate is evaporated. 100 g of a residue, containing 80percent by weight of 2-(o-nitrophenyl)-ethanol, are obtained. This residue is distilled in vacuo to obtain 70 g of 2-(o-nitrophenyl)-ethanol with a purity grade of 98percent. 45 g of o-nitrotoluene are recovered. The product is analyzed by gas chromatography. The selectivity of the reaction is 72percent, the yield of o-nitrophenylethanol is 48percent calculated for the amount of o-nitrotoluene introduced.
 

Historical Records