Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 2676865-19-1 Chemical Structure| 2676865-19-1

Structure of 2676865-19-1

Chemical Structure| 2676865-19-1

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 2676865-19-1 ]

CAS No. :2676865-19-1
Formula : C14H17NO3
M.W : 247.29
SMILES Code : O=[N+](C1=C2CCCC2=CC3=C1CC(COC)C3)[O-]
English Name :2-(Methoxymethyl)-4-nitro-1,2,3,5,6,7-hexahydro-s-indacene
MDL No. :N/A
InChI Key :VWSLCEIZIAEYDX-UHFFFAOYSA-N
Pubchem ID :162394432

Safety of [ 2676865-19-1 ]

Application In Synthesis of [ 2676865-19-1 ]

* 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 [ 2676865-19-1 ]

[ 2676865-19-1 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 496-11-7 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1.1: aluminum (III) chloride / dichloromethane / 8 h / 0 - 10 °C / Large scale 2.1: sulfuric acid / 48 h / 55 °C 2.2: 2 h / 0 - 10 °C 3.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 3.2: 16 h / 25 °C 4.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 5.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 6.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 6.2: 1 h / 20 °C
Multi-step reaction with 7 steps 1.1: aluminum (III) chloride / dichloromethane / 8 h / 0 - 10 °C / Large scale 2.1: sulfuric acid / 40 h / 55 °C 3.1: sulfuric acid; nitric acid / 1 h / 0 °C 4.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 4.2: 16 h / 25 °C 5.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 6.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 7.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 7.2: 1 h / 20 °C
  • 2
  • [ 14927-64-1 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1.1: sulfuric acid; nitric acid / 1 h / 0 °C 2.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 2.2: 16 h / 25 °C 3.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 4.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 5.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 5.2: 1 h / 20 °C
  • 3
  • [ 2676865-18-0 ]
  • [ 74-88-4 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
67% Stage #1: (4-nitro-1,2,3,5,6,7-hexahydro-s-indacen-2-yl)methanol With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 1h; 332a-d.4 Step 4 - Synthesis of 2-( methoxymethyl)-4-nitro-l, 2, 3, 5, 6, 7-hexahydro-s-indacene: To a stirred solution of (4-nitro-l,2,3,5,6,7-hexahydro-s-indacen-2-yl)methanol (350 mg, 1.5 mmol) in THF (2.0 mL) was added NaH (180 g, 4.5mmol) at 0 °C. After 30 min, Mel (0.19 mL, 4.5 mmol) was added. The reaction was wanned to room temperature. After I h, the reaction was quenched with water (20 mL). The aqueous layer was extracted with DCM (50 mL x 2). The combined organic layers were dried over anhydrous Na SCL, filtered and concentrated under reduced pressure lire crude residue was purified by flash column chromatography (silica, 15% EtOAc in petroleum ether) to give 2- (methoxymethy3)-4-nitro-l, 2, 3, 5,6, 7-hexahydro-s-indacene (250 mg , yield: 67%) as a light yellow'oil. NMR (400 MHz, CDC13): d = 7.29 (s, 1 H), 3.45-3.38 (m, 2 H), 3.37 (s, 3 H), 3.25 (t, J= 7.6 Hz, 2 H),3.11-3.01 (m, 2 H), 2.94 (t, J= 7.6 Hz, 2 H), 2.86-2.75 (m, 2 H), 2.18-2.09 (m, 2 H).
  • 4
  • [ 39105-39-0 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1.1: sulfuric acid / 48 h / 55 °C 1.2: 2 h / 0 - 10 °C 2.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 2.2: 16 h / 25 °C 3.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 4.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 5.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 5.2: 1 h / 20 °C
Multi-step reaction with 6 steps 1.1: sulfuric acid / 40 h / 55 °C 2.1: sulfuric acid; nitric acid / 1 h / 0 °C 3.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 3.2: 16 h / 25 °C 4.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 5.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 6.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 6.2: 1 h / 20 °C
  • 5
  • [ 620592-45-2 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1.1: Lithium 1,1,1,3,3,3-hexamethyldisilazide / tetrahydrofuran / 0.5 h / -78 °C 1.2: 16 h / 25 °C 2.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 3.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 4.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 4.2: 1 h / 20 °C
  • 6
  • [ 2676865-16-8 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: trifluoroacetic acid; triethylsilane / 16 h / 70 °C 2.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 3.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 3.2: 1 h / 20 °C
  • 7
  • [ 2676865-17-9 ]
  • [ 2676865-19-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: diisobutylaluminium hydride / tetrahydrofuran / 16 h / -78 - 20 °C 2.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C 2.2: 1 h / 20 °C
  • 8
  • [ 2676865-19-1 ]
  • [ 2676865-20-4 ]
YieldReaction ConditionsOperation in experiment
71% With 10% Pd/C; hydrogen In ethanol at 25℃; for 2h; 332a-d.5 Step 5 Synthesis of 2-(methoxymethyl)-l,2,3.5,6, 7 -hexahydro-s-indacen-4-amme: A mixture of 2-(methoxymethyl)-4-nitro-l,2, 3,5,6, 7-hexahydro-s-indacene (240 rng, 0.97 mmol) and 10% Pd (103 mg, 0.1 mmol) on carbon in EtOH (15mL) was stirred at 25 °C under an atmosphere of H?.. After 2 hours, the reaction mixture was filtered and concentrated to give 2- (methoxymethy3)-i,2,3,5,6,7-hexahydro-s-indacen-4-amine (0.15 g, yield: 71%) as colorless oil, which was used in the next step without further purification. MS: m/z 218.2 (M+HT).
 

Historical Records

Technical Information

Categories

Similar Product of
[ 2676865-19-1 ]

Chemical Structure| 2676865-20-4

A1497618 [2676865-20-4]

2-(Methoxymethyl)-1,2,3,5,6,7-hexahydro-s-indacen-4-amine

Reason: Derivatives