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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

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+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 7441-43-2 Chemical Structure| 7441-43-2
Chemical Structure| 7441-43-2
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Product Details of [ 7441-43-2 ]

CAS No. :7441-43-2
Formula : C9H13N
M.W : 135.21
SMILES Code : NCC1=CC=C(CC)C=C1
MDL No. :MFCD01529871
InChI Key :DGAGEFUEKIORSQ-UHFFFAOYSA-N
Pubchem ID :3870219

Safety of [ 7441-43-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 7441-43-2 ]

* 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 [ 7441-43-2 ]

[ 7441-43-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51991-94-7 ]
  • [ 7441-43-2 ]
  • C16H15N3O2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; for 16h; General procedure: A mixture of carboxylic acid (1 equiv.), amine (1 equiv.), HATU (1 equiv.) and DIPEA (3 equiv.) in DMF are stirred at room temperature or 65 C for 16 hr. Then, water is added to the reaction mixture, and the resulting mixture is filtered, and resulting solid is washed with water, and dried in vacuum to give the carboxamide product. If no solid forms when water is added to the reaction mixture, the reaction mixture may be extracted with EtOAc three times, and then the combined organic phase is washed with 10% Na2CC>3 solution, brine, dried (Na2SC>4), filtered, and evaporated to give the carboxamide product. Generally, the product is sufficiently pure (e.g., >95% purity). However, if the crude product is not sufficiently pure, then the crude product may be purified by flash chromatography.
 

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