2,4-Diamino-6-hydroxypyrimidine supplier

Name
2,4-Diamino-6-hydroxypyrimidine
EINECS 200-254-4
CAS No. 56-06-4
Article Data16
CAS DataBase
Density 1.84 g/cm³
Solubility
Melting Point 285-286 °C (dec.)(lit.)
Formula C₄H₆N₄O
Boiling Point 288.5 °C at 760 mmHg
Molecular Weight 126.118
Flash Point 128.3 °C
Transport Information
Appearance white solid
Safety 22-24/25-36-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms 4(1H)-Pyrimidinone,2,6-diamino- (8CI,9CI);2,4-Diamino-6-hydroxypyrimidine;2,4-Diamino-6-pyrimidinone;2,6-Diamino-3,4-dihydropyrimidin-4-one;2,6-Diamino-4(1H)-pyrimidinone;2,6-Diamino-4(3H)-pyrimidinone;2,6-Diamino-4-hydroxypyrimidine;2,6-Diamino-4-pyrimidinol;2,6-Diaminopyrimidin-4-one;2,6-Diaminopyrimidine-4(3H)-one;6-Aminoisocytosine;6-Hydroxy-2,4-pyrimidinediamine;NSC 44914;NSC 680818;NSC9302;
PSA 98.05000
LogP 0.50900

Synthetic route

: 506-93-4
guanidine nitrate

: 105-56-6
ethyl 2-cyanoacetate

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
Stage #1: guanidine nitrate; ethyl 2-cyanoacetate With sodium methylate In methanol for 4h; Reflux; Stage #2: With hydrogenchloride In water pH=9; pH-value;	95%

: 113-00-8
guanidine nitrate

: 105-56-6
ethyl 2-cyanoacetate

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With triethylamine In ethanol for 4h; Reflux;	66%

: 88075-70-1
2,4-diamino-5-formyl-6-oxo(1H)-pyrimidine

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With sulfuric acid In methanol for 72h; Ambient temperature;

: 108-98-5
thiophenol

: 100061-59-4
NU6038

A: 831-91-4
Benzyl phenyl sulfide

B: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With triethylamine In methanol at 60℃; Rate constant;

...Expand

: 696-83-3
2,4-diamino-6-fluoropyrimidine

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With sodium hydroxide In methanol; water at 20℃; Rate constant;

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

A: 51953-18-5
pyrimidine-4(3H)-one

B: 156-81-0
2,4-diaminopyrimidine

C: 120-89-8
parabanic acid

D: 108-53-2
isocytosine

E: 71-30-7
Cytosine

F: 144-62-7
oxalic acid

G: 113-00-8
guanidine nitrate

H: 127-17-3
2-oxo-propionic acid

I: 66-22-8
uracil

J: 56-06-4
2,6-diaminopyrimidin-4-ol

K: 66224-66-6, 66224-67-7, 66224-68-8, 66224-69-9, 134434-48-3, 134434-49-4, 134454-76-5, 134461-75-9
adenine

L: 57-13-6
urea

M: 56-40-6
glycine

Conditions

Conditions	Yield
With copper(II) choride dihydrate In water at 80℃; for 24h; pH=7.57;	A 5.6 mg B 0.3 mg C 0.59 mg D 5 mg E 0.13 mg F 0.1 mg G 1.6 mg H 0.0018 mg I 3.8 mg J 0.3 mg K 0.01 mg L 1.7 mg M 0.76 mg

...Expand

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

A: 51953-18-5
pyrimidine-4(3H)-one

B: 156-81-0
2,4-diaminopyrimidine

C: 113-00-8
guanidine nitrate

D: 66-22-8
uracil

E: 56-06-4
2,6-diaminopyrimidin-4-ol

F: 57-13-6
urea

Conditions

Conditions	Yield
With manganese(II) chloride tetrahydrate In water at 80℃; for 24h; pH=7.57;	A 0.3 mg B 0.02 mg C 0.1 mg D 0.03 mg E 0.06 mg F 0.005 mg

...Expand

: 506-93-4
guanidine nitrate

: 105-34-0
methyl 2-cyanoacetate

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With sodium methylate

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

A: 51953-18-5
pyrimidine-4(3H)-one

B: 1455-77-2
guanazole

C: 120-89-8
parabanic acid

D: 849585-22-4
LACTIC ACID

E: 73-40-5
2-amino-1,9-dihydro-6H-purin-6-one

F: 328-42-7
Oxalacetic acid

G: 2491-15-8
formylglycine

H: 110-15-6
succinic acid

I: 71-30-7
Cytosine

J: 120-73-0
purine

K: 144-62-7
oxalic acid

L: 113-00-8
guanidine nitrate

M: 127-17-3
2-oxo-propionic acid

N: 66-22-8
uracil

O: 56-06-4
2,6-diaminopyrimidin-4-ol

P: 66224-66-6, 66224-67-7, 66224-68-8, 66224-69-9, 134434-48-3, 134434-49-4, 134454-76-5, 134461-75-9
adenine

Q: 57-13-6
urea

R: 56-40-6
glycine

S: 302-72-7
rac-Ala-OH

T: 18588-61-9
2,4-diamino-pyrimidine-5-carboxylic acid

U: isocytosine

Conditions

Conditions	Yield
With ferric sulfate nonahydrate; water at 80℃; for 24h;

...Expand

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

A: 23147-58-2, 110822-84-9, 110822-85-0
glycolaldehyde dimer

B: 1455-77-2
guanazole

C: 849585-22-4
LACTIC ACID

D: 328-42-7
Oxalacetic acid

E: 110-15-6
succinic acid

F: 120-73-0
purine

G: 144-62-7
oxalic acid

H: 66-22-8
uracil

I: 56-06-4
2,6-diaminopyrimidin-4-ol

J: 57-13-6
urea

Conditions

Conditions	Yield
With copper(II) chloride tetrahydrate; water at 80℃; for 24h;

...Expand

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

A: 51953-18-5
pyrimidine-4(3H)-one

B: 120-89-8
parabanic acid

C: 73-40-5
2-amino-1,9-dihydro-6H-purin-6-one

D: 328-42-7
Oxalacetic acid

E: 110-15-6
succinic acid

F: 144-62-7
oxalic acid

G: 127-17-3
2-oxo-propionic acid

H: 56-06-4
2,6-diaminopyrimidin-4-ol

I: 57-13-6
urea

J: 18588-61-9
2,4-diamino-pyrimidine-5-carboxylic acid

K: 18514-52-8
2,3-diaminomaleonitrile

Conditions

Conditions	Yield
With water; manganese(ll) chloride at 80℃; for 24h;

...Expand

: 141-82-2
malonic acid

: 113-00-8
guanidine nitrate

: 57-13-6
urea

A: 1004-38-2
2,4,6-triaminopyrimidine

B: 4425-67-6
2-aminopyrimidine-4,6-diol

C: 67-52-7
BARBITURIC ACID

D: 108-78-1
2,4,6-triamino-s-triazine

E: 3546-50-7
pyrimidine-2,4,5-triamine

F: C4H4N2O3*C4H5N3O2

G: 56-06-4
2,6-diaminopyrimidin-4-ol

H: 31458-45-4
2-hydroxy-4,6-diaminopyrimidine

I: 2345-56-4
Malonamic acid

Conditions

Conditions	Yield
at 65℃; for 120h;

...Expand

: 50-01-1
guanidine hydrochloride

: 105-56-6
ethyl 2-cyanoacetate

: 56-06-4
2,6-diaminopyrimidin-4-ol

Conditions

Conditions	Yield
With sodium ethanolate In ethanol at 50 - 70℃; under 1500.15 Torr; for 1.5h; Large scale;

: 20099-89-2
4-Cyanophenacyl bromide

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 4-(2-amino-4-hydroxy-7H-pyrrolo[2,3-d]pyrimidin-6-yl)benzonitrile

Conditions

Conditions	Yield
Stage #1: 2,6-diaminopyrimidin-4-ol With sodium acetate In water at 100℃; for 0.333333h; Stage #2: 4-Cyanophenacyl bromide In methanol at 100℃;	100%
Stage #1: 2,6-diaminopyrimidin-4-ol With sodium acetate In water at 100℃; for 0.333333h; Stage #2: 4-Cyanophenacyl bromide In methanol; water at 100℃;	100%

: 333-20-0
potassium thioacyanate

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 22288-75-1
2,4-diamino-6-hydroxy-5-thiocyanatopyrimidine

Conditions

Conditions	Yield
Stage #1: potassium thioacyanate; 2,6-diaminopyrimidin-4-ol With acetic acid at 25 - 95℃; Inert atmosphere; Stage #2: With bromine at 10 - 20℃; for 2h;	100%

: 2698-41-1
o-chlorobenzylidene malononitrile

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 2,7-diamino-3,4-dihydro-4-oxo-5-(2-chlorophenyl)pyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With N-benzyl-N,N,N-triethylammonium chloride In water at 90℃; for 5h;	99%

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 6312-72-7
5-bromo-2,4-diamino-6-hydroxypyrimidine

Conditions

Conditions	Yield
With bromine; sodium hydrogencarbonate In methanol; water 2 h stirring, then standing overnight;	97%
With N-Bromosuccinimide; montmorillonite K-10; tetrabutylammomium bromide for 0.0416667h; microwave irradiation;	92%

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 2387-48-6
2,4-diamino-5-nitroso-6-hydroxypyrimidine

Conditions

Conditions	Yield
With acetic acid; sodium nitrite In water at 80℃;	97%
With acetic acid; sodium nitrite In water	97%

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 3346-23-4
2,4-diamino-5-nitro-6-hydroxypyrimidine

Conditions

Conditions	Yield
With sulfuric acid; nitric acid at 30 - 35℃; for 2h;	96.4%
With sodium nitrite In water at 0 - 5℃; under 750.075 Torr; for 0.5h; Large scale;

: 138911-94-1
2-hydroxymethylene-1-tetralone sodium salt

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 10-amino-8-oxo-9H-5,6-dihydrobenzopyrimido<5,4-b>quinoline

Conditions

Conditions	Yield
With phosphoric acid at 100℃; for 90h;	95%

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 488-17-5
3-methylbenzene-1,2-diol

: 2-amino-5-methyl-9H-pyrimido[4,5-b]indole-4,6,7-triol

Conditions

Conditions	Yield
In aq. phosphate buffer at 20℃; pH=7; Electrolysis; Green chemistry;	95%

: 959934-74-8
3-[(2-methyl-4-oxo-4H-chromen-8-yl)methylene]pentane-2,4-dione

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 959934-79-3
8-(6-acetyl-2-amino-4-hydroxy-7-methyl-5,8-dihydropyrido[2,3-d]-pyrimidin-5-yl)-2-methyl-4H-chromen-4-one

Conditions

Conditions	Yield
In isopropyl alcohol for 48h; Reflux; Inert atmosphere;	94%

: 437-81-0
2,6-difluorobenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(2,6-difluorophenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.133333h;	94%

...Expand

: 120-80-9
benzene-1,2-diol

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 2-amino-9H-pyrimido[4,5-b]indole-4,6,7-triol

Conditions

Conditions	Yield
In aq. phosphate buffer at 20℃; pH=7; Electrolysis; Green chemistry;	93%

: 34036-07-2
3,4 difluorobenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(3,4-difluorophenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.216667h;	92%

...Expand

: 1122-91-4
4-bromo-benzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(4-bromophenyl)-3,4,5,8-tetrahydro-4-oxopyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.183333h;	92%

...Expand

: europium(III) nitrate hydrate

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 857036-63-6
Eu((NH2)2C4N2H2O)2(H2O)3(NO3)2(1+)*NO3(1-)=Eu((NH2)2C4N2H2O)2(H2O)3(NO3)3

Conditions

Conditions	Yield
In methanol pyrimidine-compound was added to methanol, then hydrated Eu(NO3)3 was added, the soln. was stirred for 24 h; slow evapd.; elem. anal.;	91%

: 934-00-9
3-methocycatechol

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 2-amino-5-methoxy-9H-pyrimido[4,5-b]indole-4,6,7-triol

Conditions

Conditions	Yield
In aq. phosphate buffer at 20℃; pH=7; Electrolysis; Green chemistry;	91%

: 104-88-1
4-chlorobenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(4-chlorophenyl)-3,4,5,8-tetrahydro-4-oxopyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.166667h;	91%

...Expand

: 105-07-7
4-cyanobenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(4-cyanophenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.216667h;	91%

...Expand

: terbium(III) chloride hydrate

: 56-06-4
2,6-diaminopyrimidin-4-ol

: Tb((NH2)2C4N2H2O)2(H2O)6(3+)*3Cl(1-)=Tb((NH2)2C4N2H2O)2(H2O)6Cl3

Conditions

Conditions	Yield
In methanol pyrimidine-compound was added to methanol, then hydrated TbCl3 was added, the soln. was stirred for 24 h; slow evapd.; elem. anal.;	90.4%

: 2700-23-4
4-Nitrobenzylidenemalononitrile

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 2,7-diamino-3,4-dihydro-4-oxo-5-(4-nitrophenyl)pyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With N-benzyl-N,N,N-triethylammonium chloride In water at 90℃; for 6h;	90%

: 100-52-7
benzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-4-oxo-5-phenyl-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.3h;	90%

...Expand

: 3132-99-8
m-bromobenzoic aldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(3-bromophenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.2h;	90%

...Expand

: 83-38-5
2,6-dichlorobenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(2,6-dichlorophenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.2h;	90%

...Expand

: C12H13NO4

: 56-06-4
2,6-diaminopyrimidin-4-ol

: C16H19N5O5

Conditions

Conditions	Yield
In water; ethyl acetate at 50℃; for 24h;	90%

: 2051-49-2
n-hexanoic anhydride

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 1402591-91-6
N,N'-(6-hydroxypyrimidine-2,4-diyl)dihexanamide

Conditions

Conditions	Yield
for 4h; Reflux;	89%

: 89-98-5
2-chloro-benzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(2-chlorophenyl)-3,4,5,8-tetrahydro-4-oxopyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.233333h;	89%

...Expand

: 99-61-6
3-nitro-benzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(3-nitrophenyl)-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.266667h;	89%

...Expand

: 121-32-4
4-hydroxy-3-ethoxybenzaldehyde

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 109-77-3
malononitrile

: 2,7-diamino-5-(3-ethoxy-4-hydroxyphenyl)-4-oxo-3,4,5,8-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile

Conditions

Conditions	Yield
With silica-coated iron oxide nanomagnetic particles-bonded S-sulfonic acid In neat (no solvent) at 100℃; for 0.333333h;	89%

...Expand

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 154597-38-3
(4RS)-4-ethyl-7,8-dihydro-4-hydroxy-7-dimethylaminomethylene-1H-pyrano<3,4-f>indolizine-3,6,10(4H)-trione

: (4RS)-8-amino-4-ethyl-4-hydroxy-1H-pyrano<3'',4'':6',7'>indolizino<2',1':5,6>pyrido<2,3-d>pyrimidine-3,10,14(4H,9H,12H)-trione

Conditions

Conditions	Yield
In acetic acid for 20h; Heating;	88%

: 956-04-7
3-(4-chlorophenyl)-1-phenylprop-2-en-1-one

: 56-06-4
2,6-diaminopyrimidin-4-ol

: 5-(4-chlorophenyl)-7-phenyl-4-oxo-5,8-dihydropyrido<2,3-d>pyrimidine

Conditions

Conditions	Yield
With aluminum oxide; potassium fluoride In ethanol at 80℃; for 0.666667h;	88%

2,4-Diamino-6-hydroxypyrimidine Specification

The IUPAC name of 2,4-Diamino-6-hydroxypyrimidine is 2,6-diamino-1H-pyrimidin-4-one. With the CAS registry number 56-06-4, it is also named as 4(1H)-Pyrimidinone, 2,6-diamino-. The product's categories are Pyrimidine; APIs & Intermediate; Pyridines, Pyrimidines, Purines and Pteredines; Chemical Amines; 13C & 2H Sugars; Amines; Bases & Related Reagents; Heterocycles; Nucleotides; Carbohydrates & Derivatives, and the other registry numbers are 40306-60-3; 41982-31-4; 863767-89-9. Besides, it is white solid, which should be stored in sealed, dark, cool, ventilated and dry place away from fire and heat source. In addition, it is light sensitive.

The other characteristics of this product can be summarized as: (1)EINECS: 200-254-4; (2)ACD/LogP: -1.66; (3)# of Rule of 5 Violations: 1; (4)ACD/LogD (pH 5.5): -1.66; (5)ACD/LogD (pH 7.4): -1.66; (6)ACD/BCF (pH 5.5): 1; (7)ACD/BCF (pH 7.4): 1; (8)ACD/KOC (pH 5.5): 2.95; (9)ACD/KOC (pH 7.4): 2.98; (10)H bond acceptors: 5; (11)H bond donors: 5; (12)Freely Rotating Bonds: 1; (13)Index of Refraction: 1.798; (14)Molar Refractivity: 29.21 cm³; (15)Molar Volume: 68.4 cm³; (16)Surface Tension: 94.7 dyne/cm; (17)Density: 1.84 g/cm³; (18)Flash Point: 128.3 °C; (19)Melting point: 285-286 °C; (20)Enthalpy of Vaporization: 52.78 kJ/mol; (21)Boiling Point: 288.5 °C at 760 mmHg; (22)Vapour Pressure: 0.00232 mmHg at 25 °C.

Preparation of 2,4-Diamino-6-hydroxypyrimidine: please put Guanidine nitrate in the solution of Sodium methoxide (or 50% NaOH) to heat and stir. After backflow half-hour, please drop Methyl cyanoacetate to reflow 2 hours. After the reaction complete, please heat the reclaimed Methanol. And then put the residues in the hot water to dissolve. When the temperature reach 80 °C, please add acetic acid to adjust pH=8. Then please separate crystallographic product out. After cooling below 20 °C, you would get this chemical by filtration, washing and drying.

Uses of 2,4-Diamino-6-hydroxypyrimidine: it is used for detection of nitrate and nitrite. It is also used in organic synthesis and pharmaceutical intermediates. And it is used for the production of AZM, minoxidilum and olic acid. Furthermore, it can react with 1,3-Dichloro-propan-2-one to get 5-Chloromethyl-furo[2,3-d]pyrimidine-2,4-diamine.

This reaction needs Dimethylformamide at temperature of 20 °C for 24 hours. The yield is 80 %.

When you are using this chemical, please be cautious about it as the following: it is irritating to eyes, respiratory system and skin. Please do not breathe dust. And please avoid contact with skin and eyes. You should wear suitable protective clothing. Moreover, in case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

People can use the following data to convert to the molecule structure.
(1)SMILES:O=C/1/N=C(/N)NC(\N)=C\1
(2)InChI:InChI=1/C4H6N4O/c5-2-1-3(9)8-4(6)7-2/h1H,(H5,5,6,7,8,9)
(3)InChIKey:SWELIMKTDYHAOY-UHFFFAOYAR
(4)Std. InChI:InChI=1S/C4H6N4O/c5-2-1-3(9)8-4(6)7-2/h1H,(H5,5,6,7,8,9)
(5)Std. InChIKey:SWELIMKTDYHAOY-UHFFFAOYSA-N

Product Name

2,4-Diamino-6-hydroxypyrimidine

Synthetic route

2,4-Diamino-6-hydroxypyrimidine Specification

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