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| 181130-14-3 Chemical Structure| 181130-14-3

Structure of 181130-14-3

Chemical Structure| 181130-14-3

*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 [ 181130-14-3 ]

CAS No. :181130-14-3
Formula : C7H7N3
M.W : 133.15
SMILES Code : N#CC1=NC=C(CN)C=C1
MDL No. :MFCD08457627

Safety of [ 181130-14-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P301+P310
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 181130-14-3 ]

* 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 [ 181130-14-3 ]

[ 181130-14-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 71760-04-8 ]
  • [ 38675-10-4 ]
  • [ 181130-14-3 ]
  • [ 181130-15-4 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate; c) Boc-D-phenylalanylproline (6-cyano-3-picolyl)amide 8.12 g of diisopropylethylamine and subsequently 11 ml (15 mmol) of propanephosphonic anhydride (50% strength solution in ethyl acetate) were added dropwise to a solution of 2.11 g (12.5 mmol) of 2-cyano-5-(aminomethyl)pyridine and 4.5 g (12.5 mmol) of <strong>[38675-10-4]Boc-D-Phe-Pro-OH</strong> in 70 ml of CH2Cl2 at -5 C. The mixture was then stirred for 2 h, during which the temperature was allowed to rise from -5 to 20 C. The organic phase was washed with water, 5% strength sodium bicarbonate and 5% strength citric acid solutions, dried over Na2SO4 and evaporated to dryness. A pale yellowish crystalline residue was obtained, melting point 167-170 C., and was used without further purification in the next reaction.
  • 2
  • [ 71760-04-8 ]
  • [ 38675-10-4 ]
  • [ 181130-14-3 ]
  • Boc-(D)-phenylalanylproline (6-cyano)-3-picolylamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate; c Boc-(D)-phenylalanylproline (6-cyano)-3-picolylamide 8.12 g of diisopropylethylamine, and subsequently 11 ml (15 mmol) of propanephosphonic anhydride (50% strength solution in ethyl acetate), were added dropwise to a solution of 2.11 g (12.5 mmol) of 2-cyano-5-(aminomethyl)pyridine and 4.5 g (12.5 mmol) of <strong>[38675-10-4]Boc-D-Phe-Pro-OH</strong> in 70 ml of CH2 Cl2 at -5 C. The mixture was then stirred for 2 h, allowing the temperature to rise from -5 to 20 C. The organic phase was washed with water, 5% strength sodium bicarbonate and 5% strength citric acid solutions, dried over Na2 SO4 and evaporated to dryness, a pale yellowish crystalline residue was obtained, melting point 167-170 C., which was used in the next reaction without further purification.
 

Historical Records

Technical Information

Categories