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1,4-Benzodioxane-6-aldehyde

Names

[ CAS No. ]:
29668-44-8

[ Name ]:
1,4-Benzodioxane-6-aldehyde

[Synonym ]:
1,4-Benzodioxin-6-carboxaldehyde, 2,3-dihydro-
2,3-dihydro-1,4-benzodioxin-6-carboxaldehyde
3,4-Ethylenedioxybenzaldehyde
MFCD00010092
1,4-Benzodioxin-6-carboxaldehyde,2,3-dihydro
1,4-Benzodioxan-6-carbaldehyde
EINECS 249-763-3
2,3-dihydro-1,4-benzodioxine-6-carbaldehyde
2,3-dihydro-benzo[1,4]dioxine-6-carbaldehyde
1,4-benzodioxan-6-carboxaldehyde
6-Formyl-1,4-benzodioxane
3,4-ethylene dioxybenzaldehyde
2H,3H-benzo[e]1,4-dioxin-6-carbaldehyde
2,3-dihydrobenzo[b][1,4]dioxine-6-carbaldehyde
2,3-dihydro-benzo[1,4]dioxin-6-carboxaldehyde
1,4-Benzodioxane-6-aldehyde
1,4-Benzodioxane-6-carboxaldehyde

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
221.2±0.0 °C at 760 mmHg

[ Melting Point ]:
50-52 °C(lit.)

[ Molecular Formula ]:
C9H8O3

[ Molecular Weight ]:
164.158

[ Flash Point ]:
116.0±7.9 °C

[ Exact Mass ]:
164.047348

[ PSA ]:
35.53000

[ LogP ]:
1.54

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.588

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2932999099

Synthetic Route

Customs

[ HS Code ]: 2932999099

[ Summary ]:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

New technique for high-throughput synthesis.

Bioorg. Med. Chem. Lett. 9(9) , 1305-10, (1999)

A new technique for high throughput solid phase synthesis using the centrifuge based liquid removal from readily available standard microtiterplates is described. This technique eliminates the filtrat...

A practical approach to new (5Z) 2-alkylthio-5-arylmethylene-1-methyl-1,5-dihydro-4H-imidazol-4-one derivatives.

Molecules 16(9) , 7377-90, (2011)

A practical protocol for the preparation of (5Z)-2-alkylthio-5-arylmethylene-1-methyl-1,5-dihydro-4H-imidazol-4-one derivatives is reported. The new compounds were obtained in good yield and stereosel...

Structure-activity relationships involving the catechol subunit of rolipram. Stafford JA, et al.

Bioorg. Med. Chem. Lett. 4(15) , 1855-60, (1994)


More Articles


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