5-nitro-2-furfural diacetate

5-nitro-2-furfural diacetate structural formula

Structural formula

Business number 024W
Molecular formula C9H9NO7
Molecular weight 243.17
label

5-Nitrofuryl methylene diethyl ester,

2-(acetylmethyl)-5-nitrofuran,

5-Nitrofurfural diacetyl acetal,

5-Nitro-2-furanmethandiol diacetate,

Heterocyclic compounds

Numbering system

CAS number:92-55-7

MDL number:MFCD00003244

EINECS number:202-166-1

RTECS number:LU1940000

BRN number:255089

PubChem ID:None

Physical property data

1. Properties: white crystalline powder or granules.

2. Density (g/mL, 25/4?): Undetermined

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 90?92

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined Determined

10. Autoignition point or ignition temperature (ºC): Not determined

11. Vapor pressure (kPa, 25ºC): Not determined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit ( %, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Undetermined

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 52.09

2. Molar volume (cm3/mol): 174.1

3. Isotonic specific volume (90.2K ): 460.8

4. Surface tension (dyne/cm): 49.0

5. Polarizability (10-24cm3): 20.65

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 7

4. Number of rotatable chemical bonds: 5

5. Number of tautomers: none

6. Topological molecule polar surface area 112

7. Number of heavy atoms: 17

8. Surface charge: 0

9. Complexity: 308

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. The number of uncertain stereocenters of atoms: 0

13. The number of determined stereocenters of chemical bonds: 0

14. The number of uncertain stereocenters of chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

Low toxicity. Microsomal mutation test: Typhimurium 10?g/plate. See furfural.
?

Storage method

This product should be sealed and stored away from light.

Packaged in iron drums or plywood drums lined with plastic bags. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to general chemical product regulations.

Synthesis method

It is obtained by nitration and esterification of furfural. Add acetic anhydride to the reaction pot, cool it to -5°C, add 1/5 of the added amount of mixed acid (nitric acid and sulfuric acid) dropwise, and then add a mixture of nitric acid and furfural (1:2 volume) dropwise at the same time, and control the temperature at At about 0?, after adding it for about 5-6 hours, continue to add a part of furfural dropwise. Then, stir for 1 hour, add water and sodium carbonate solution, raise the temperature to 55-62°C, and keep it warm for 1 hour. Cool to 15°C, filter, wash with water, and spin dry to obtain the finished product, with a yield of 85%.

Purpose

It is a pharmaceutical intermediate, used in the preparation of furan anti-infective drugs (furatolin, nitrofuracillin, furantantine, etc.).

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1-phenylpiperazine

1-phenylpiperazine structural formula

Structural formula

Business number 024V
Molecular formula C10H14N2
Molecular weight 162.23
label

N-phenylpiperazine,

N-Phenyldiethylenediamine

Numbering system

CAS number:92-54-6

MDL number:MFCD00005957

EINECS number:202-165-6

RTECS number:TM2625000

BRN number:132157

PubChem number:24898377

Physical property data

1. Characteristics: Undetermined

2. Density (g/mL, 25/4?): 1.062

3. Relative vapor density (g/mL, air = 1): Undetermined

4. Melting point (ºC): 18.8

5. Boiling point (ºC, normal pressure): 286

6. Boiling point (ºC ,5.2kPa): Undetermined

7. Refractive index: 1.5865-1.5885

8. Flash point (ºC): 140

9. Specific rotation (º): Undetermined

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V/V): Undetermined

18. Explosion lower limit (%, V/V): Undetermined

19. Solubility: Undetermined

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 49.80

2. Molar volume (cm3/mol): 157.7

3. Isotonic specific volume (90.2K ): 388.9

4. Surface tension (dyne/cm): 36.9

5. Polarizability (10-24cm3): 19.74

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 15.3

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 124

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be kept sealed.

Synthesis method

Prepared by dehydration and cyclization of 2-(2-aminoethylamino)-2-phenylethanol [H2NCH2CH2NHCH(C6H5)CH2OH] in an autoclave at 220°C.

Purpose

Starting raw materials for the synthesis of 2-phenylpiperazine compounds. The ones that have been synthesized include 1,4-dimethyl-2-phenylpiperazine and 1,4-diethyl-2-phenyl. Piperazine, 1-ethyl-2-phenylpiperazine and a series of compounds.

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4-Phenylmorpholine

4-Phenylmorpholine Structural Formula

Structural formula

Business number 024U
Molecular formula C10H13NO
Molecular weight 163.22
label

N-phenylmorpholine,

4-Phenylmorpholine,

(4-Morpholinyl)benzene,

N-Phenylmorpholine,

anti-corrosion additives,

catalyst,

Multifunctional solvent

Numbering system

CAS number:92-53-5

MDL number:MFCD00006166

EINECS number:202-164-0

RTECS number:QE8575000

BRN number:None

PubChem number:24852668

Physical property data

1. Properties: colorless crystals.

2. Density (g/mL, 57/20?): 1.06

3. Relative vapor density (g/mL, air=1): 5.63

4. Melting point (ºC): 57

5. Boiling point (ºC, normal pressure): 268

6. Boiling point (ºC, 5.999kPa): 165~170

p>

7. Flash point (ºC, open): 104

8. Vapor pressure (kPa, 20ºC): <0.013

9. Solubility: soluble in ethanol , diethyl ether, insoluble in water.

Toxicological data

The oral LD50 in rats is 930mg/kg.

Ecological data

None

Molecular structure data

1. Molar refractive index: 48.06

2. Molar volume (cm3/mol): 152.7

3. Isotonic specific volume (90.2K ): 381.0

4. Surface tension (dyne/cm): 38.7

5. Polarizability (10-24cm3): 19.05

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 1

5. Number of tautomers: none

6. Topological molecule polar surface area 12.5

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 126

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

N-Phenylmorpholine is a fairly stable compound and does not easily catch fire. Chemical properties pKa 3.20 (25°C, water). Condensation with benzaldehyde produces a colorless matrix, which is rearranged to obtain malachite green dye. Due to the presence of morpholino group, the ortho-para position of the benzene ring is activated and reacts with nitric acidObtain ortho and para nitro compounds. It is relatively stable to oxidation and only generates a small amount of formaldehyde when oxidized with dichromic acid.

Storage method

This product should be kept sealed.

Synthesis method

Prepared from the action of N, N-bis-?-hydroxyethylaniline and sulfuric acid.

Purification method: Use water for recrystallization and purification.

Purpose

The compound has properties similar to N, N-dimethylaniline and is basic. It can be used as a reagent for dehydrobromination of allyl bromide compounds and has the advantage that the product is easier to purify. Used as anti-corrosion additives, intermediates for dyes and insecticides, and catalysts in the decomposition of peroxides.

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