5-nitro-2-furaldehyde semicarbazone 5-nitro-2-furaldehyde semicarbazone

5-nitro-2-furfural semicarbazide structural formula

5-nitro-2-furfural semicarbazide structural formula

structural formula

business number 01aq
molecular formula c6h6n4o4
molecular weight 198.14
label

nitrofurazone,

furacin,

nfz,

nitrofurazone

numbering system

cas number:59-87-0

mdl number:mfcd00003225

einecs number:200-443-1

rtecs number:lt7700000

brn number:86403

pubchem number:24886543

physical property data

1. characteristics: yellow crystalline powder.

2. density (g/ml,25/4℃): undetermined

3. relative steam density (g/ml,air=1) : undetermined

4. melting point (ºc):236 -240℃ (decomposition).

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 optical rotation (º): undetermined

10. autoignition point or ignition temperature (ºc): undetermined

11. vapor pressure (kpa,25ºc): undetermined

12. 43.56

2. molar volume (m3/mol):116.0

3. isotonic specific volume (90.2k):348.1

4. surface tension (dyne/cm):81.0

5. polarizability(10-24cm3):17.27

compute chemical data

1. reference value for hydrophobic parameter calculation (xlogp): none

2. number of hydrogen bond donors: 2

3. number of hydrogen bond acceptors: 5

4. number of rotatable chemical bonds: 2

5. number of tautomers: 3

6. topological molecule polar surface area 126

7. number of heavy atoms: 14

8. surface charge: 0

9. complexity: 261

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: 1

14. number of uncertain chemical bond stereocenters: 0

15. number of covalent bond units: 1

properties and stability

none yet

storage method

prepared from furfural through nitration, esterification and hydrolysis5-nitrofurfural, and then condensed with amino hydrochloride to obtain nitrofurazone.

synthesis method

prepared from furfural through nitration, esterification and hydrolysis5-nitrofurfural, and then condensed with amino hydrochloride to obtain nitrofurazone.

purpose

this product is a nitrofuran antibacterial drug. this class of drugs also includes furazolidone and nitrofurantoin. nitrofuracillin is highly toxic when taken orally and is used for local or surface disinfection in surgery.

: 0cm 0cm 0pt; text-align: left; mso-pagination: wi-orphan; mso-margin-top-alt: auto; mso-margin-bottom-alt: auto” align=left>by furfural is prepared through nitration, esterification and hydrolysis5- span>nitrofurfural is condensed with the amino acid hydrochloride to obtain nitrofuracillin.

synthesis method

prepared from furfural through nitration, esterification and hydrolysis5-nitrofurfural, and then condensed with amino hydrochloride to obtain nitrofurazone.

purpose

this product is a nitrofuran antibacterial drug. this class of drugs also includes furazolidone and nitrofurantoin. nitrofuracillin is highly toxic when taken orally and is used for local or surface disinfection in surgery.

bdmaee:bis (2-dimethylaminoethyl) ether

cas no:3033-62-3

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