Home Cart Sign in  
HazMat Fee +

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| 73278-98-5 Chemical Structure| 73278-98-5

Structure of 73278-98-5

Chemical Structure| 73278-98-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 73278-98-5 ]

CAS No. :73278-98-5
Formula : C15H24N2O
M.W : 248.36
SMILES Code : NCCCOC1=CC=CC(CN2CCCCC2)=C1
MDL No. :MFCD07787282

Safety of [ 73278-98-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H335-H314
Precautionary Statements:P260-P264-P270-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P405-P501
Class:8
UN#:3259
Packing Group:

Application In Synthesis of [ 73278-98-5 ]

* 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 [ 73278-98-5 ]

[ 73278-98-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 73278-98-5 ]
  • [ 4224-62-8 ]
  • 6-Chloro-hexanoic acid [3-(3-piperidin-1-ylmethyl-phenoxy)-propyl]-amide [ No CAS ]
  • 2
  • [ 73278-98-5 ]
  • [ 4922-68-3 ]
  • N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,2,4-triazolo[4,3-a]pyridine-3-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With ammonia; In ethanol; dichloromethane; (a) N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,2,4-triazolo-[4,3-a]pyridine-3-amine 3-Bromo-1,2,4-triazolo[4,3-a]pyridine (2.5 g), 3-[3-(1-piperidinylmethyl)phenoxy]propanamine (9 g) and ethanol (20 ml) were heated in an autoclave at 110 for 24 h and then at 150 for 36 h. The mixture was evaporated in vacuo (200, 0.1 mm Hg) and the residue (2.3 g) was chromatographed on silica using dichloromethane:ethanol:880 ammonia (100:8:1) to give a gum which was crystallized from methyl acetate-petroleum ether (b.p. 60-80) to give the title compound (0.8 g) as white crystals, m.p. 150-151. Found: C, 69.0; H, 7.4; N, 19.1; C21 H27 N5 O requires: C, 69.0; H, 7.45; N, 19.2%.
  • 3
  • [ 73278-98-5 ]
  • [ 62473-92-1 ]
  • N-[3-[3-[(1-piperidinyl)methyl]phenoxy]propyl]-6-bromo-1,2-benzisothiazol-3-amine 1,1-dioxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With phosphorus pentachloride; In 6-bromo-3-chlorobenzo[d]isothiazole 1,1-dioxide; 1,2-dichloro-benzene; acetonitrile; EXAMPLE 14 N-[3-[3-[(1-piperidinyl)methyl]phenoxy]propyl]-6-bromo-1,2-benzisothiazol-3-amine 1,1-dioxide, hydrochloride A mixture of 4.00 g (15 mmol) <strong>[62473-92-1]6-bromo-1,2-benzisothiazol-3(2H)-one 1,1-dioxide</strong> and 3.57 g (17 mmol) phosphorus pentachloride in 5 ml o-dichlorobenzene is heated from ambient temperature to 160° C. over one hour and is held at that temperature for one additional hour. Upon cooling, liquids are removed in vacuo and the residual 6-bromo-3-chlorobenzisothiazole 1,1-dioxide is suspended in acetonitrile and added portionwise to a solution of 3.7 g (15 mmol) 3-[3-[(1-piperidinyl)methyl]phenoxy]propylamine in refluxing acetonitrile. Heating at reflux is continued for one hour after completion of the addition, after which the reaction mixture is cooled to room temperature. The solution is decanted away from a small quantity of gum and the solvent is removed on a rotoevaporator. The resulting oil is dissolved in absolute ethanol, from which the title compound precipitates. m.p. 217°-220° C. IR (KBr) 1625, 1290, 1165, 1150 cm-1
 

Historical Records

Technical Information

Categories