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| 79-77-6 Chemical Structure| 79-77-6
Chemical Structure| 79-77-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 79-77-6

,{[proInfo.pro_purity]}

(E)-β-Ionone is the isomer of β-Ionone . β-Ionone is effective in the induction of apoptosis in gastric adenocarcinoma SGC7901 cells. β-Ionone has anti-cancer activity

Synonyms: β-Lonone

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 (E)-β-Ionone

CAS No. :79-77-6
Formula : C13H20O
M.W : 192.30
SMILES Code : CC(/C=C/C1=C(C)CCCC1(C)C)=O
Synonyms :
β-Lonone
MDL No. :MFCD00001549
InChI Key :PSQYTAPXSHCGMF-BQYQJAHWSA-N
Pubchem ID :638014

Safety of (E)-β-Ionone

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

Application In Synthesis of (E)-β-Ionone

* 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 [ 79-77-6 ]

[ 79-77-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2346-00-1 ]
  • [ 79-77-6 ]
  • [ 55089-94-6 ]
  • 3
  • [ 79-77-6 ]
  • [ 14150-94-8 ]
  • 2-[2-(2,6,6-trimethylcyclohexen-1-yl)ethenyl]-5-nitropyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
79% With ammonium acetate; In ethanol; at 80℃; for 6h;Microwave irradiation; General procedure: To a solution of the dinitropyridone 1 (50 mg, 0.25 mmol) in ethanol (10 mL), 4-phenyl-3-buten-2-one (4a) (36.5 mg, 0.25 mmol) and NH4OAc (578 mg, 7.5 mmol) were added, and the resultant mixture was heated at 65 C for 24 h. After removal of the solvent, the residue was washed with benzene (3 × 10 mL) to remove unreacted ketone 4a and treated with column chromatography on silica gel (eluent: hexane/ethyl acetate =95/5) to afford 5-nitro-2-(2-phenylethenyl)pyridine (5a) (41 mg, 0.18 mmol, 72%) as a yellow powder. The reactions of the dinitropyridone 1 with other ketones 4b-f or 10a-c were performed in a similar way.
 

Historical Records

Technical Information

Categories