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Chemical Structure| 18378-20-6 Chemical Structure| 18378-20-6
Chemical Structure| 18378-20-6

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BBD is a biochemical reagent/chromogenic reagent.

Synonyms: NSC240867; Benzylamino-NBD

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of BBD

CAS No. :18378-20-6
Formula : C13H10N4O3
M.W : 270.24
SMILES Code : O=[N+](C1=CC=C(NCC2=CC=CC=C2)C3=NON=C31)[O-]
Synonyms :
NSC240867; Benzylamino-NBD
English Name :N-Benzyl-7-nitrobenzo[c][1,2,5]oxadiazol-4-amine
MDL No. :MFCD00038006
InChI Key :GZFKJMWBKTUNJS-UHFFFAOYSA-N
Pubchem ID :87615

Safety of BBD

Application In Synthesis of BBD

* 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 [ 18378-20-6 ]

[ 18378-20-6 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 5714-17-0 ]
  • [ 100-46-9 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
In ethanol
  • 2
  • [ 10199-89-0 ]
  • [ 100-46-9 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
64% With tertiary amine In acetonitrile for 16h; Reflux; Inert atmosphere; General SNAr Procedure to Prepare Compounds 10074-G5 and 3a - 3q General procedure: To a solution of 4-chloro-7-nitrobenzofurazan (NBD-Cl, 2; 1 eq.) in acetonitrile (0.1 M) was added the requisite amine (1.1 eq.) followed by triethylamine (2 eq.) The reaction mixture was then stirred at reflux under an inert atmosphere (N2) for 16 h. The solvent was removed in vacuo, then the residue was re-dissolved in EtOAc, washed with 1 M HCl, water, brine, dried (Na2SO4), filtered and concentrated. The crude material was purified over silica gel, eluting with a gradient of EtOAc in Hexanes.
60% In methanol
In ethanol
YieldReaction ConditionsOperation in experiment
64% With triethylamine In acetonitrile for 16h; Reflux; Inert atmosphere; General Procedure to Prepare Compounds 10074- G5 and3a-3q General procedure: To a solution of 4-chloro-7-nitrobenzoliirazan (NBD-Cl, 2; 1 eq.) in acetonitrile (0.1 M) was added the requisite amine (1.1 eq.) followed by triethylamine (2 eq.). The reaction mixture was then stirred at reflux under an inert atmosphere (N2) for 16 h. The solyent was remoyed in yacuo, then the residue was re-dissolyed in EtOAc, washed with 1 M HC1, water, brine, dried (Na2 S04), fltered and concentrated. The crude material was purifed oyer silica gel, eluting with a gradient ofEtOAc in Hexanes.
7-Chlornitrobenzoxadiazol, Benzylamin;
7-Chlor-4-nitro-benzofurazan, Benzylamin (RT);
  • 4
  • [ 17348-69-5 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: (i) NH2OH*HCl, EtOH, H2O, (ii) KOH 2: HNO3, H2SO4 3: ethanol
  • 5
  • [ 1635-61-6 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: KOH, NaOCl / aq. ethanol 2: (i) NH2OH*HCl, EtOH, H2O, (ii) KOH 3: HNO3, H2SO4 4: ethanol
  • 6
  • [ 1194-66-7 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: (i) NaN3, DMSO, (ii) (heating) 2: HNO3, H2SO4 3: ethanol
  • 7
  • [ 19155-86-3 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: HNO3, H2SO4 2: ethanol
  • 8
  • [ 7116-16-7 ]
  • [ 18378-20-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: HNO3, H2SO4 2: ethanol
 

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