Home Cart Sign in  
Chemical Structure| 58331-11-6 Chemical Structure| 58331-11-6

Structure of 58331-11-6

Chemical Structure| 58331-11-6

*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 [ 58331-11-6 ]

CAS No. :58331-11-6
Formula : C4H3ClIN3O
M.W : 271.44
SMILES Code : O=C1N=C(N)NC(Cl)=C1I

Safety of [ 58331-11-6 ]

Application In Synthesis of [ 58331-11-6 ]

* 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 [ 58331-11-6 ]

[ 58331-11-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1194-21-4 ]
  • [ 58331-11-6 ]
YieldReaction ConditionsOperation in experiment
In N-methyl-acetamide; PREPARATION 7 2-Amino-5-iodo-6-chloro-4-pyrimidinol To 1.45 grams (10.0 millimoles) of 6-chloro-isocytosine is added 15 ml. of dimethylformamide (DMF) and 2.27 grams (10.08 millimoles) of N-iodosuccinimide. With protection from external moisture, the mixture is heated on a steam bath for one-hour hour. The resulting brownish red solution is allowed to stand overnight at room temperature with continued exclusion of moisture. The solution is evaporated under reduced pressure and the residual solid azeotroped once with ethanol in vacuo. The resulting solid is triturated with glacial acetic acid. The insoluble solid is collected, washed with a small volume of glacial acetic acid, then with acetone. The solid is re-triturated with glacial acetic acid, collected, washed with acetone and air-dried. Yield, 1.50 g. Evaporation of the combined filtrate in vacuo, trituration of the residue with water, then acetone gives, after collecting and drying, 970 mg. of second-crop material. The first-crop material is crystallized twice from glacial acetic acid to give 540 mg. of 2-amino-5-iodo-6-chloro-4-pyrimidinol which decomposes at >270°, has lambdamax0.1N NaOh 236 nm. (epsilon9,150); 285 nm. (epsilon6,200) and the infrared absorption below. NH/CH, 3380, 3300, 3190, 3130; O=O/C=C/C=N/NH deformation, 1670v.s., 1580, 1540; C--N/Other, 1320, 1215, 1010; Other, 910, 755 cm-1. Analysis Calcd. for: C4 H3 CllN3 O: C, 17.73; H, 1.11; Cl, 13.08; l, 46.83; N, 15.51. Found: C, 18.51; H, 2.24; Cl, 13.38; l, 46.50; N, 14.70.
In N-methyl-acetamide; EXAMPLE 5 2-Amino-5-iodo-6-chloro-4-pyrimidinol To 1.45 grams (10.0 millimoles) of <strong>[1194-21-4]6-chloroisocytosine</strong> is added 15 ml. of dimethylformamide (DMF) and 2.27 grams (10.08 millimoles) of N-iodosuccinimide. With protection from external moisture, the mixture is heated on a steam bath for one-half hour. The resulting brownish red solution is allowed to stand overnight at room temperature with continued exclusion of moisture. The solution is evaporated under reduced pressure and the residual solid azeotroped once with ethanol in vacuo. The resulting solid is triturated with glacial acetic acid. The insoluble solid is collected, washed with a small volume of glacial acetic acid, then with acetone. The solid is re-triturated with glacial acetic acid, collected, washed with acetone and air dried. Yield, 1.50 g. Evaporation of the combined filtrate in vacuo, trituration of the residue with water, then acetone gives, after collecting and drying, 970 mg. of secondcrop material. The first-crop material is crystallized twice from glacial acetic acid to give 540 mg. of 2-amino-5-iodo-6-chloro-4-pyrimidinol which decomposes at >270°, has a lambdamax0.1N NaOH 236 nm (epsilon9,150); 285 nm (epsilon6,200) and the infrared absorption below. Nh/ch, 3380, 3300, 3190, 3130; o=o/c=c/c=n/nh deformation, 1670v.s., 1580, 1540; C--N/Other, 1320, 1215, 1010; Other, 910, 755 cm-1. Analysis Calcd. for: C4 H3 ClIN3 O: C, 17.73; H, 1.11; Cl, 13.08; I, 46.83; N, 15.51. Found: C, 18.51; H, 2.24; Cl, 13.38; I, 46.50; N, 14.70.
 

Historical Records

Technical Information

Categories