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[ CAS No. 4499-86-9 ]

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type HazMat fee
Excepted Quantity Free
Ground (Domestic only) Free
Inaccessible (Haz class 6.1), Domestic USD 41.00
Inaccessible (Haz class 6.1), International USD 64.00
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 83.00
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2D
Chemical Structure| 4499-86-9
Chemical Structure| 4499-86-9
Structure of 4499-86-9 *Storage: {[proInfo.prStorage]}

Quality Control of [ 4499-86-9 ]

Purity: {[proInfo.showProBatch.pb_purity]}

Related Doc. of [ 4499-86-9 ]

SDS

Product Details of [ 4499-86-9 ]

CAS No. :4499-86-9MDL No. :MFCD00009360
Formula :C12H29NOBoiling Point :-
Linear Structure Formula :-InChI Key :N/A
M.W :203.36Pubchem ID :20586
Synonyms :

Computed Properties of [ 4499-86-9 ]

TPSA : - H-Bond Acceptor Count : -
XLogP3 : - H-Bond Donor Count : -
SP3 : - Rotatable Bond Count : -

Safety of [ 4499-86-9 ]

Signal Word:DangerClass8
Precautionary Statements:P280-P305 P351 P338-P310UN#:3267
Hazard Statements:H314Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4499-86-9 ]

  • Downstream synthetic route of [ 4499-86-9 ]

[ 4499-86-9 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 4499-86-9 ]
  • 2,5-poly-3-(hexyl-6-phosphonic acid)thiophene; monomer(s): 2-bromo-3-(hexyl(6-diethyl phosphonate))-5-(tributylstannyl)thiophene [ No CAS ]
  • 2,5-poly-3-(hexyl-6-phosphonic acid)thiophene, tetrapropylammonium salt; monomer(s): 2-bromo-3-(hexyl(6-diethyl phosphonate))-5-(tributylstannyl)thiophene [ No CAS ]
  • 2
  • [ 4499-86-9 ]
  • poly(3-dodecyl-3\-(6-hexylphosphonic acid)-5,2\-bithiophene); monomer(s): diethyl 6-(5\-bromo-4\-dodecyl-5-(tributylstannyl)-2,2\-bithien-3-yl)hexylphosphonate [ No CAS ]
  • poly(3-dodecyl-3\-(6-hexylphosphonic acid)-5,2\-bithiophene), tetrapropylammonium salt; monomer(s): diethyl 6-(5\-bromo-4\-dodecyl-5-(tributylstannyl)-2,2\-bithien-3-yl)hexylphosphonate [ No CAS ]
  • 3
  • [ 151-21-3 ]
  • [ 4499-86-9 ]
  • tetrapropylammonium dodecyl sulfate [ No CAS ]
  • 4
  • [ 634-63-9 ]
  • [ 11113-50-1 ]
  • [ 4499-86-9 ]
  • C8H12BN4O8(1-)*C12H28N(1+) [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% In ethanol; water; at 60℃; for 3h; l-Tartramide(2 mmol, 300 mg), boric acid (1 mmol, 62 mg) and tetra-npropylammoniumhydroxide (40% in water), [NPr4][OH](1 mmol, ca 0.5 ml), were combined in ethanol (2 ml) andheated at 60 C for 3 h. The product was obtained aftercooling and allowing evaporation over a period of 2 d. Theresulting white crystalline solids were filtered off and washedwith a small amount of cold dioxane and dried, giving 350 mgof 1 (71% yield). A suitable colourless block-shaped crystalwas chosen for single-crystal X-ray diffraction.
  • 5
  • C69H69N13O6 [ No CAS ]
  • [ 4499-86-9 ]
  • 12C12H28N(1+)*4O4P(3-)*4C69H69N13O6 [ No CAS ]
  • 6
  • C69H69N13O6 [ No CAS ]
  • [ 4499-86-9 ]
  • 12C12H28N(1+)*4O4P(3-)*4C69H69N13O6 [ No CAS ]
  • 7
  • C66H63N13O6 [ No CAS ]
  • [ 4499-86-9 ]
  • 12C12H28N(1+)*4O4P(3-)*4C66H63N13O6 [ No CAS ]
  • 8
  • C66H63N13O6 [ No CAS ]
  • [ 4499-86-9 ]
  • 12C12H28N(1+)*4O4P(3-)*4C66H63N13O6 [ No CAS ]
  • 9
  • [ 458-37-7 ]
  • [ 4499-86-9 ]
  • tetrapropylammonium curcumin salt [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; water; at 25℃; for 8h; 0.50 g of curcumin was added to a 50 mL round bottom flask, and 10 mL of ethanol was added to completely dissolve the raw material, and then 1.3 g of a [4499-86-9]tetrapropylammonium hydroxide aqueous solution was added in a molar ratio of curcumin to [4499-86-9]tetrapropylammonium hydroxide (1:1). 25%),After vigorous neutralization at 25 C for 8 h of acid-base neutralization, the solvent was removed by rotary evaporation to obtain a reddish brown tetrapropyl curcumin ammonium salt ionic liquid.
  • 10
  • [ 7631-95-0 ]
  • [ 5970-45-6 ]
  • [ 13362-78-2 ]
  • [ 4499-86-9 ]
  • [ 10294-56-1 ]
  • [ 7439-98-7 ]
  • Mo12O40PH3Zn4*3C12H10N2 [ No CAS ]
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