What is the 3,4-Diaminofurazan?

3,4-Diaminofurazan is white to slightly beige crystalline powder, while it's Molecular Formula is C2H4N4O. white to slightly beige crystalline powder 3,4-Diaminofurazan is a building block used to prepare magnesium and zinc alkynylated salicylaldehyde-diamine Schiff base complexes. 3,4-Diaminofurazan is also used to prepare aryl(hydroxy)oxadiazolopyrazines via oxidation of acetophenones followed by heterocyclization with antibacterial-activities.

What is the CAS number for 3,4-Diaminofurazan?

The CAS number of 3,4-Diaminofurazan is 17220-38-1.

What is 3,4-Diaminofurazan (17220-38-1) used for?

3,4-Diaminofurazan is a white to slightly beige crystalline powder that serves as a versatile building block in the synthesis of various chemical compounds. It is known for its ability to form complexes with metals such as magnesium and zinc, and it also plays a role in the creation of aryl(hydroxy)oxadiazolopyrazines with antibacterial properties.InChI:InChI=1/C4H6N2O/c5-3-1-7-2-4(3)6/h1-2H,5-6H2

What is the 3,4-Diaminofurazan?

3,4-Diaminofurazan is white to slightly beige crystalline powder, while it's Molecular Formula is C2H4N4O. white to slightly beige crystalline powder 3,4-Diaminofurazan is a building block used to prepare magnesium and zinc alkynylated salicylaldehyde-diamine Schiff base complexes. 3,4-Diaminofurazan is also used to prepare aryl(hydroxy)oxadiazolopyrazines via oxidation of acetophenones followed by heterocyclization with antibacterial-activities.

What is the CAS number for 3,4-Diaminofurazan?

The CAS number of 3,4-Diaminofurazan is 17220-38-1.

What is 3,4-Diaminofurazan (17220-38-1) used for?

3,4-Diaminofurazan is a white to slightly beige crystalline powder that serves as a versatile building block in the synthesis of various chemical compounds. It is known for its ability to form complexes with metals such as magnesium and zinc, and it also plays a role in the creation of aryl(hydroxy)oxadiazolopyrazines with antibacterial properties.InChI:InChI=1/C4H6N2O/c5-3-1-7-2-4(3)6/h1-2H,5-6H2

Product classification

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17220-38-1

Product Name:3,4-Diaminofurazan
Molecular Formula:C₂H₄N₄O
Molecular Weight:100.08
Appearance:white to slightly beige crystalline powder

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Product Details

pd_meltingpoint:178-183 °C

Appearance:white to slightly beige crystalline powder

Purity:99%

Top quality factory supply 17220-38-1 3,4-Diaminofurazan at low price

Molecular Formula:C2H4N4O
Molecular Weight:100.08
Appearance/Colour:white to slightly beige crystalline powder
Vapor Pressure:0.056mmHg at 25°C
Melting Point:178-183 °C
Refractive Index:1.621
Boiling Point:304 °C at 760 mmHg
PKA:1.31±0.47(Predicted)
Flash Point:137.7 °C
PSA：90.96000
Density:1.582 g/cm³
LogP:0.39640

3,4-Diaminofurazan(Cas 17220-38-1) Usage

InChI:InChI=1/C4H6N2O/c5-3-1-7-2-4(3)6/h1-2H,5-6H2

17220-38-1 Relevant articles

Taming of 3,4-Di(nitramino)furazan

Tang, Yongxing,Zhang, Jiaheng,Mitchell, Lauren A.,Parrish, Damon A.,Shreeve, Jeanne M.

, p. 15984 - 15987 (2015)

Highly energetic 3,4-di(nitramino)furaza...

3,3′-Dinitroamino-4,4′-azoxyfurazan and its derivatives: An assembly of diverse N-O building blocks for high-performance energetic materials

Zhang, Jiaheng,Shreeve, Jean'Ne M.

, p. 4437 - 4445 (2014)

On the basis of a design strategy that r...

N-trinitroethyl-substituted azoxyfurazan: High detonation performance energetic materials

Yu, Qiong,Wang, Zhixin,Yang, Hongwei,Wu, Bo,Lin, Qiuhan,Ju, Xuehai,Lu, Chunxu,Cheng, Guangbin

, p. 27305 - 27312 (2015)

Azoxyfurazan derivatives based on the tr...

Tetracyclic pyrazine-fused furazans as insensitive energetic materials: Syntheses, structures, and properties

Sun, Qi,Li, Xin,Lin, Qiuhan,Lu, Ming

, p. 8034 - 8037 (2018)

Energetic compounds with fused tetracycl...

A study of N-trinitroethyl-substituted aminofurazans: High detonation performance energetic compounds with good oxygen balance

Yu, Qiong,Wang, Zhixin,Wu, Bo,Yang, Hongwei,Ju, Xuehai,Lu, Chunxu,Cheng, Guangbin

, p. 8156 - 8164 (2015)

Two energetic N-trinitroethyl-substitute...

A Two-Step Synthesis of Diaminofurazan and Synthesis of N-Monoarylmethyl and N,N'-Diarylmethyl Derivatives

Zelenin, Alexander K.,Trudell, Mark L.

, p. 1057 - 1060 (1997)

Diaminofurazan (1) was synthesized from ...

-

Komin,A.P. et al.

, p. 2749 - 2752 (1975)

Tetrazine-furazan ring high-nitrogen energetic compound and synthesis method thereof

-

Paragraph 0015; 0027-0029, (2020/11/25)

The invention relates to a tetrazine-fur...

Kilogram-grade preparation method of 3,3'-diamino-4,4'-azoxyfurazan

-

Paragraph 0043; 0047; 0051; 0058; 0066; 0073; 0080; 0087, (2019/02/03)

The invention discloses a kilogram-grade...

17220-38-1 Process route

: 131543-46-9,107-22-2
Glyoxal

: 17220-38-1
3,4-diaminofurazan

Conditions

Conditions	Yield
With hydroxylamine hydrochloride; urea; sodium hydroxide; In water; at 105 ℃; for 2h;	67%
Glyoxal; With hydroxylamine hydrochloride; sodium hydroxide; In water; at 108 ℃; for 7h; Cooling with ice; With urea; In water; at 100 - 110 ℃; for 24h; Temperature;	50%
With hydroxylamine hydrochloride; urea; sodium hydroxide; In water; at 110 ℃;	45%
With hydroxylamine hydrochloride; urea; at 102 - 108 ℃;
With hydroxylamine hydrochloride; urea; at 102 - 108 ℃;
With hydroxylamine hydrochloride; urea; sodium hydroxide; at 125 ℃; for 15h;
With hydroxylamine hydrochloride; urea; sodium hydroxide; at 105 ℃; for 15h;

: 2580-79-2
diaminoglyoxime

: 17220-38-1
3,4-diaminofurazan

Conditions

Conditions	Yield
With potassium hydroxide; at 170 - 180 ℃; for 2h;	70%
With potassium hydroxide; for 0.333333h; microwave irradiation;	70%
With potassium hydroxide; In ethylene glycol; at 120 - 170 ℃; for 1h; Product distribution / selectivity;	52%
In ethylene glycol; at 165 ℃; for 0.5h; Product distribution / selectivity;	52%
With potassium hydroxide; at 170 ℃; for 2h;	50%
With sodium hydroxide; at 165 ℃;
With sodium hydroxide; In N,N-dimethyl-formamide; for 4h; Ambient temperature;
With potassium hydroxide; at 180 ℃;
at 165 ℃; for 0.5h; Product distribution / selectivity; Neat (no solvent);
With potassium hydroxide; In water;

17220-38-1 Upstream products

2580-79-2
diaminoglyoxime
120493-20-1
5-trifluoromethyl-1,2,4-oxadiazole-3-carboxyamidoxime
120493-21-2
3,3’-bi-(5-trifluoromethyl-1,2,4-oxadiazole)
606-23-5
1H-indene-1,3(2H)-dione

17220-38-1 Downstream products

67200-28-6
5-(4-chloro-phenyl)-[1,2,5]oxadiazolo[3,4-b]pyrazine
26261-74-5
5,7-diphenyl-4H-[1,2,5]oxadiazolo[3,4-b][1,4]diazepine
67200-30-0
5-(4-methoxyphenyl)furazano[3,4-b]pyrazine
140706-48-5
3-amino-4-benzamidofurazan

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