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[ CAS No. 2516-93-0 ]

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Chemical Structure| 2516-93-0
Chemical Structure| 2516-93-0
Structure of 2516-93-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2516-93-0 ]

CAS No. :2516-93-0 MDL No. :MFCD00067044
Formula : C6H12O3 Boiling Point : 239.5°C at 760 mmHg
Linear Structure Formula :- InChI Key :N/A
M.W :132.16 g/mol Pubchem ID :41958
Synonyms :

Safety of [ 2516-93-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P234-P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P390-P405-P406-P501 UN#:3265
Hazard Statements:H290-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2516-93-0 ]

  • Downstream synthetic route of [ 2516-93-0 ]

[ 2516-93-0 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 64-17-5 ]
  • [ 2516-93-0 ]
  • [ 14144-70-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride
  • 2
  • [ 2516-93-0 ]
  • [ 92-69-3 ]
  • [ 54334-90-6 ]
YieldReaction ConditionsOperation in experiment
With naphthalene-2-sulfonate; xylene
  • 3
  • [ 2516-93-0 ]
  • [ 103860-77-1 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride Erhitzen des Reaktionsprodukts mit <i>sec</i>-Butylalkohol;
  • 4
  • [ 3926-62-3 ]
  • [ 2372-45-4 ]
  • [ 2516-93-0 ]
  • 5
  • [ 79-11-8 ]
  • [ 2372-45-4 ]
  • [ 2516-93-0 ]
  • 6
  • [ 2516-93-0 ]
  • [ 137-07-5 ]
  • 2-butoxymethyl-benzothiazole [ No CAS ]
  • 7
  • [ 10228-54-3 ]
  • [ 2516-93-0 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide
  • 8
  • [ 124-38-9 ]
  • [ 2351-69-1 ]
  • [ 2516-93-0 ]
YieldReaction ConditionsOperation in experiment
(i) Mg, I2, HgCl2, dimethoxymethane, (ii) /BRN= 1900390/; Multistep reaction;
  • 9
  • [ 2516-93-0 ]
  • [ 56680-70-7 ]
YieldReaction ConditionsOperation in experiment
92% With thionyl chloride In dichloromethane at 0 - 20℃; for 2h; 2.1. Synthesis of 2-alkoxyacetyl chlorides 9A-D General procedure: 2-Alkoxyacetic acid [5A-D: 5A (0.225 g, 2.5 mmol, 0.230 ml), 5B (0.237 g, 2.3 mmol, 0.245 ml), 5C (0.248 g, 2.1 mmol, 0,250 ml) or 5D (0.925 g, 7.0 mmol, 0.930 ml)] was dissolved in dichloromethane (10 mL) in a dry round-bottom flask at 0 °C. A solution of thionyl chloride (1.0 equiv.) in dichloromethane (10 mL) was added dropwise at 0 °C and the resulted mixture was stirred at 0 °C for 1 h and at RT for 1 h. After removal of solvent and other volatiles in vacuum to afford the corresponding 2-alkoxyacetyl chloride 9A-D as colorless oil.
With thionyl chloride
  • 10
  • [ 105-36-2 ]
  • [ 71-36-3 ]
  • [ 2516-93-0 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride In tetrahydrofuran
  • 11
  • [ 2516-93-0 ]
  • [ 481-42-5 ]
  • 3-butoxymethylplumbagin [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% With lead(IV) acetate In benzene for 8h; Heating;
  • 12
  • [ 79-11-8 ]
  • [ 71-36-3 ]
  • [ 2516-93-0 ]
YieldReaction ConditionsOperation in experiment
24% With sodium butanolate at 80℃; for 0.166667h;
With sodium hydride In tetrahydrofuran
YieldReaction ConditionsOperation in experiment
Rk. mit CH2N2;
YieldReaction ConditionsOperation in experiment
at 15℃; Veresterung;
at 25℃; Veresterung;
at 35℃; Veresterung;
YieldReaction ConditionsOperation in experiment
Chloressigsaeure, Na-Butylat, Butanol, Sieden;
n-Butoxyglycidather, AgO/ NaOH;
Na-Butylat, 1. Butanol-(1), 60grad, 2. Chloressigsaeure, Siedetemp., 1.5 h;
1 Preparation 1 Preparation 1 3-oxaheptanoic acid Sodium metal (16 g) was added to 92.5 ml of butanol and heated at reflux under nitrogen. After the sodium had reacted, chloroacetic acid (32.9 g) in 40 ml of butanol was added dropwise and then heated at reflux for twenty hours. The mixture, upon cooling to room temperature, was added to 1300 ml of water and extracted four times with 250-ml portions of diethyl ether. The aqueous phase was acidified to about pH 2 with aqueous hydrochloric acid and again extracted four times with 250-ml portions of diethyl ether. The organic extracts were combined and dried over sodium sulfate, filtered, and concentrated in vacuo. Distillation afforded the title compound as an oil. Structure assignment was supported by the proton nmr spectrum.

  • 16
  • [ 2516-93-0 ]
  • [ 6148-64-7 ]
  • γ-butoxyacetoacetic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
Stage #1: 2-butoxyacetic acid With 1,1'-carbonyldiimidazole In tetrahydrofuran Stage #2: ethyl potassium malonate With magnesium chloride In tetrahydrofuran
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