成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart Sign in  
Chemical Structure| 822-55-9 Chemical Structure| 822-55-9

Structure of 822-55-9

Chemical Structure| 822-55-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 822-55-9

,{[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 2 weeks

  • {[ 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 [ 822-55-9 ]

CAS No. :822-55-9
Formula : C4H6N2O
M.W : 98.10
SMILES Code : OCC1=CNC=N1
MDL No. :MFCD00266718
InChI Key :QDYTUZCWBJRHKK-UHFFFAOYSA-N
Pubchem ID :1745

Safety of [ 822-55-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 822-55-9 ]

* 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 [ 822-55-9 ]

[ 822-55-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 822-55-9 ]
  • [ 17289-25-7 ]
  • [ 38993-84-9 ]
  • 2
  • [ 822-55-9 ]
  • [ 1072-84-0 ]
  • 3
  • [ 1072-84-0 ]
  • [ 822-55-9 ]
YieldReaction ConditionsOperation in experiment
In sulfuric acid; EXAMPLE 2 A solution of 4-imidazolecarboxylic acid (0.56 g) in 25percent v/v sulphuric acid (25 cc) was placed in the cathodic compartment of a vessel as described in example 1, and 25percent v/v sulphuric acid was placed in the anodic compartment. The mixture was electrolysed for 31/2 hours under conditions similar to those described in Example 1. The solution from the cathodic compartment was neutralised with potassium carbonate (18.5 g) and the mixture was evaporated to dryness. The solid residue was extracted with hot isopropanol (200 cc) and the extract was evaporated to an oil which was crystallized from ether to give 4-(hydroxymethyl)imidazole (0.42 g) m.p. 66°-80°. The picrate derivative of this material was recrystallized from water and had m.p. 205.5°.
  • 4
  • [ 822-55-9 ]
  • [ 454-16-0 ]
  • [ 1077629-45-8 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In acetonitrile;Reflux; Example 27(l-{4-[4-(2-Chloro-pyridin-3-yloxy)-6-methoxy-[l,3,5]triazin-2-ylamino]-2-methoxy- phenyl}-lH-imidazol-4-yl)-methanola) [ 1 -(2-Methoxy-4-nitro-phenyl)- 1 H-imidazo 1-4-yl] -methano 1A mixture of l-fluoro-2-methoxy-4-nitro-benzene (1.0 g, 5.8 mmol), (1 H-imidazo 1-4-yl)- methanol (602 mg, 6.1 mmol) and cesium carbonate (2.86 g, 8.8 mmol) in 40 ml of acetonitrile was refluxed overnight. The reaction mixture was concentrated in vacuo, diluted with water and extracted with ethyl acetate. Chromatography on Si-NH2 (Isolute) using ethyl acetate as an eluent gave the title compound as a yellowish solid.MS ISP (m/e): 250.1 (51) [(M+H)+]1H NMR (CDCl3, 300 MHz): delta (ppm) = 8.00-7.85 (m, 3H), 7.45 (d, 1 H), 7.26 (d, IH), 4.70 (s, 2H), 4.01 (s, 3H).
With potassium carbonate; In N,N-dimethyl-formamide; at 100℃; for 16h; Example A37 a) Preparation of intermediate 98 A mixture of l-fluoro-2-methoxy-4-nitrobenzene (2.45 g, 14.3 mmol), 4- hydroxymethyl- IH- imidazole (1.54 g, 15.7 mmol) and K2CO3 (3.95 g, 28.6 mmol) in DMF (20 ml) was stirred at 100 0C for 16 h. The mixture was concentrated in vacuo, and the residue was partitioned between EtOAc and water. Undissolved material was collected by filtration and dissolved in a mixture of TEtaF and CEta3CN. The combined organic layers were dried (MgSO4), filtered and the solvent was evaporated. The residue was triturated in DIPE/2-propanol, filtered off and dried. Yield: 1.2 g of intermediate 98 which was used as such in the next reaction step.
 

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 822-55-9 ]

Alcohols

Chemical Structure| 17289-25-7

A180800 [17289-25-7]

(1-Methyl-1H-imidazol-4-yl)methanol

Similarity: 0.93

Chemical Structure| 38585-62-5

A124098 [38585-62-5]

(4-Methyl-1H-imidazol-5-yl)methanol hydrochloride

Similarity: 0.80

Chemical Structure| 38993-84-9

A301953 [38993-84-9]

(1-Methyl-1H-imidazol-5-yl)methanol

Similarity: 0.70

Chemical Structure| 82090-52-6

A970240 [82090-52-6]

Imidazo[1,2-a]pyridin-2-ylmethanol

Similarity: 0.61

Chemical Structure| 78892-28-1

A229123 [78892-28-1]

(2,6-Dimethylphenyl)(1H-imidazol-4-yl)methanol

Similarity: 0.58