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[ CAS No. 56-10-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 56-10-0
Chemical Structure| 56-10-0
Structure of 56-10-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 56-10-0 ]

CAS No. :56-10-0 MDL No. :MFCD00037011
Formula : C3H11Br2N3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 281.01 Pubchem ID :-
Synonyms :
2-Aminoethyl Carbamimidothioate Dihydrobromide

Safety of [ 56-10-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 56-10-0 ]

* 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 [ 56-10-0 ]

[ 56-10-0 ] Synthesis Path-Downstream   1~11

  • 4
  • [ 75-15-0 ]
  • [ 56-10-0 ]
  • [ 18470-70-7 ]
YieldReaction ConditionsOperation in experiment
(i) aq. NH3, (ii) /BRN= 1098293/; Multistep reaction;
  • 5
  • [ 56-10-0 ]
  • [ 543-18-0 ]
YieldReaction ConditionsOperation in experiment
(i) aq. Ba(OH)2, (ii) O2; Multistep reaction;
  • 6
  • [ 56-10-0 ]
  • 2-Guanidinoaethyl-2-guanidino-aethanthiolsulfinat [ No CAS ]
YieldReaction ConditionsOperation in experiment
With ammonium hydroxide; dihydrogen peroxide
  • 7
  • [ 56-10-0 ]
  • 2-Guanidinoaethyl-2-guanidinoaethanthiolsulfonat Dihydrobromid [ No CAS ]
YieldReaction ConditionsOperation in experiment
(i) aq. Ba(OH)2, (ii) aq. H2O2, I2, H2SO4; Multistep reaction;
  • 8
  • [ 56-10-0 ]
  • [ 114935-55-6 ]
  • [ 114472-79-6 ]
YieldReaction ConditionsOperation in experiment
50% In water for 0.5h;
  • 9
  • [ 2576-47-8 ]
  • [ 17356-08-0 ]
  • [ 56-10-0 ]
YieldReaction ConditionsOperation in experiment
In N,N-dimethyl-formamide at 80℃; other temperatures, ΔH(excit.), ΔS(excit.);
In ethanol at 80℃; other β-substituted bromoethanes; ΔH(excit.), ΔS(excit.); var. temp.; mechanism;
YieldReaction ConditionsOperation in experiment
Rk. in wss. Ba(OH)2 mit O2/30grad, 2h -> 2-Guanidino-ethansulfonsaeure;
Rk. in wss. Ba(OH)2 mit H2SO4 in W., H2O2 und wenig I2/30grad, 2d -> 2-Guanidino- ethyl-2-guanidinoethanthiolsulfonat-2HBr;
Umlagerg. in II u. III;
With water
With water Radiolysis;

  • 11
  • [ 1415635-39-0 ]
  • [ 56-10-0 ]
  • [ 1415635-15-2 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine In butan-1-ol for 0.5h; Reflux; 61 Example 61[0280] The chloropteridine (852 mg, 2.5 X 10"3 moles) was stirred in n-butanol (20 mL) and S-(2-aminoethyl)isothiourea dihydrobromide (1.41 gm, 5.0 X 10"3 moles) along with diisopropylethylamine (1.3 gm, 0.01 moles) were added. This mixture was heated at reflux for 30 minutes. The reaction was diluted with diethyl ether (200 mL) and this mixture was extracted with 5% hydrochloric acid (2 X 100 mL). The combined aqueous extracts were washed with diethyl ether (100 mL) before being made basic by the addition of potassium carbonate. The product separated as a pale yellow solid. This solid was isolated by filtration and washed with water to provide, after drying, 961 mg of the product as a yellow solid.LC/MS: M+1 = 424.21.
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