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[ CAS No. 1210-96-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 1210-96-4
Chemical Structure| 1210-96-4
Structure of 1210-96-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1210-96-4 ]

CAS No. :1210-96-4 MDL No. :MFCD00454170
Formula : C8H8N2O6 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 228.16 Pubchem ID :-
Synonyms :

Safety of [ 1210-96-4 ]

Signal Word:Danger Class:4.1,6.1
Precautionary Statements:P240-P210-P241-P280-P370+P378-P501-P261-P270-P271-P264-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405 UN#:2926
Hazard Statements:H228-H301+H311+H331-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1210-96-4 ]

* 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 [ 1210-96-4 ]

[ 1210-96-4 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 4920-84-7 ]
  • [ 1210-96-4 ]
YieldReaction ConditionsOperation in experiment
With nitric acid
  • 2
  • [ 85238-99-9 ]
  • [ 1210-96-4 ]
  • [ 4920-84-7 ]
  • (2,4-dimethoxy-5-nitrophenyl)isopropyl ketone [ No CAS ]
  • (1-acetoxy-2-methylpropyl)-2,4-dimethoxy-5-nitrobenzene [ No CAS ]
YieldReaction ConditionsOperation in experiment
1: 16% 2: 18% 3: 53% 4: 60% With nitric acid In acetic acid at -5℃; for 1h; Further byproducts given;
1: 30% 2: 7% 3: 35% 4: 58% With nitric acid In acetic acid at 20℃; for 1h; Further byproducts given;
  • 3
  • [ 704-14-3 ]
  • [ 1210-96-4 ]
Reference: [1],,p. 238
  • 4
  • [ 610-38-8 ]
  • [ 1210-96-4 ]
  • 6
  • [ 3698-83-7 ]
  • 1,3-Dimethgxy-4,6-dinitrobenzene [ No CAS ]
  • [ 1210-96-4 ]
YieldReaction ConditionsOperation in experiment
90% With hydrogenchloride; In methanol; water; EXAMPLE 2 Preparing 1,3-Dimethgxy-4,6-dinitrobenzene from <strong>[3698-83-7]1,3-Dichloro-4,6-dinitrobenzene</strong> STR6 A 1-liter, 3-necked, round-bottomed flask is charged with 500 mL of methanol, 30 g of crushed potassium hydroxide, 75 mL of water, and 23.7 g (0.10 mole) of 1,3-dichloro-4,6-dinitrobenzene. The reaction mixture is agitated and heated to 65 C. for 8 hours and cooled to 25 C. The reaction mixture is then quenched with an excess of 0 C. aqueous hydrochloric acid. The resulting pale yellow solid is isolated by filtration and air-dried to yield 20 g (90% yield) of 1,3-dimethoxy-4,6-dinitrobenzene, a diether of dinitroresorcinol.
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