Home Cart Sign in  
Chemical Structure| 51768-01-5 Chemical Structure| 51768-01-5

Structure of 51768-01-5

Chemical Structure| 51768-01-5

*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 [ 51768-01-5 ]

CAS No. :51768-01-5
Formula : C7H3ClN4
M.W : 178.58
SMILES Code : N#CC1=CC(C#N)=C(Cl)N=C1N
MDL No. :MFCD00204019

Safety of [ 51768-01-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 51768-01-5 ]

* 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 [ 51768-01-5 ]

[ 51768-01-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 51768-01-5 ]
  • [ 78473-10-6 ]
YieldReaction ConditionsOperation in experiment
73% EXAMPLE 3 2-Amino-3,5-dicyanopyridine (5) was prepared from 3 using the procedure described below for the preparation of 5 except that 5 was recrystallized from MeCN [methyl cyanide; acetonitrile) (instead of EtOH). The yield was 73% (7.00 g from 12.0 g (67.2 mmol) of 3] of product homogeneous on TLC (cyclohexane-EtOAc, 1:1); mp 220 C. dec; 1 H NMR (Me2 SO-d6) delta7.90 (s, NH2), 8.40 and 8.58 (two d, 4-H and 6H, J=2 Hz).
palladium; In 1,4-dioxane; Step A 2-amino-3.5-dicyanopyridine A mixture of 2-amino-6-chloro-3,5-dicyanopyridine (Synth. Comm. 1993, 2605, 15.0 g, 84 mmol) and 10% palladium on carbon (10.0 g) in dioxane (150 mL) was shaken on a Parr apparatus under hydrogen (55 psi) for 16 h. More catalyst (7.5 g) was added and after a further 4 h the reaction mixture was filtered through celite washing through with ethanol and evaporated in vacuo. The residue was partitioned between methylene chloride and 1 M HCl. The insoluble material was collected by filtration and dried to give the title compound. The methylene chloride layer was washed with brine, dried (Na2SO4) and evaporated in vacuo to give additional product: 1H NMR (DMSO) delta 7.93 (br s, 2H), 8.41 (d, J=2.2 Hz, 1H), 8.56 (d, J=2.2 Hz, 1H).
 

Historical Records

Technical Information

Categories