Home Cart Sign in  
Chemical Structure| 50901-43-4 Chemical Structure| 50901-43-4

Structure of 50901-43-4

Chemical Structure| 50901-43-4

*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 [ 50901-43-4 ]

CAS No. :50901-43-4
Formula : C5H6N2O
M.W : 110.11
SMILES Code : OCC1=CC=NN=C1
MDL No. :MFCD06227446
InChI Key :GXWAGVFGTPTYAO-UHFFFAOYSA-N
Pubchem ID :13316256

Safety of [ 50901-43-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 50901-43-4 ]

* 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 [ 50901-43-4 ]

[ 50901-43-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34231-77-1 ]
  • [ 50901-43-4 ]
YieldReaction ConditionsOperation in experiment
33% With sodium tetrahydroborate; In methanol; for 1h; The methyl ester 15 (0.133 g, 0.963 mmol) was added to an oven dried 20 mL reactionvial followed by methanol (12 mL). Sodium borohydride (0.073 g, 1.93 mmol) was added and the reaction stirred for 1 h.A sample aliquot was taken from the reaction, quenched with sat. ammonium chloride, dissolved in 1 mL HPLC gradeMeCN, and analyzed with LC-MS to confirm the completion of the reaction. The reaction was quenched with sat.ammonium chloride and condensed to dryness to give a white solid. After condensing, DCM (100 mL) was added to theflask and the white solids were broken up and sonicated for 10 min, then vacuum filtered through a paper filter. The motherliquor was concentrated to give a yellow oil. The oil was dissolved with DCM and purified by flash chromatography (5 gSiO2 cartridge; 0-12% MeOH/DCM gradient) to give the title compound as a yellow oil (0.035 g, 33%). This compoundhas been previously reported and characterized (CAS 50901-43-4). 1H NMR (300 MHz, CDCl3) delta = 4.85 (s, 2H), 7.60 (dd,J = 5.3, 2.4 Hz, 1H), 9.06 (d, J = 5.3 Hz, 1H), 9.15 (s, 1H).
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 50901-43-4 ]

Alcohols

Chemical Structure| 1956324-99-4

A379058 [1956324-99-4]

(5-Methylpyridazin-4-yl)methanol

Similarity: 0.94

Related Parent Nucleus of
[ 50901-43-4 ]

Pyridazines

Chemical Structure| 1956324-99-4

A379058 [1956324-99-4]

(5-Methylpyridazin-4-yl)methanol

Similarity: 0.94

Chemical Structure| 38283-35-1

A393494 [38283-35-1]

4,5-Dimethylpyridazine

Similarity: 0.81