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6313-33-3

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6313-33-3 Usage

Chemical Properties

White solid

Uses

5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).

Check Digit Verification of cas no

The CAS Registry Mumber 6313-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6313-33:
(6*6)+(5*3)+(4*1)+(3*3)+(2*3)+(1*3)=73
73 % 10 = 3
So 6313-33-3 is a valid CAS Registry Number.
InChI:InChI=1/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H

6313-33-3 Well-known Company Product Price

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  • Aldrich

  • (268607)  Formamidinehydrochloride  97%

  • 6313-33-3

  • 268607-5G

  • 817.83CNY

  • Detail
  • Aldrich

  • (268607)  Formamidinehydrochloride  97%

  • 6313-33-3

  • 268607-25G

  • 2,335.32CNY

  • Detail

6313-33-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Formamidine Hydrochloride

1.2 Other means of identification

Product number -
Other names methanimidamide,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6313-33-3 SDS

6313-33-3Synthetic route

1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Methylamino-but-2-enoic acid ethyl ester; hydrochloride

(E)-3-Methylamino-but-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-methylpyrimidine-5-carboxylate
110960-73-1

ethyl 4-methylpyrimidine-5-carboxylate

C

4-Methylamino-nicotinic acid ethyl ester

4-Methylamino-nicotinic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Product distribution; Mechanism; Heating; further N-substituted enaminone hydrochlorides;A n/a
B 7%
C 45%
In acetonitrile for 6h; Heating;A n/a
B 7%
C 45%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Ethylamino-but-2-enoic acid ethyl ester; hydrochloride

(E)-3-Ethylamino-but-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-methylpyrimidine-5-carboxylate
110960-73-1

ethyl 4-methylpyrimidine-5-carboxylate

C

4-Ethylamino-nicotinic acid ethyl ester

4-Ethylamino-nicotinic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 6%
C 38%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Piperidin-1-yl-but-2-enoic acid ethyl ester; hydrochloride

(E)-3-Piperidin-1-yl-but-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-methylpyrimidine-5-carboxylate
110960-73-1

ethyl 4-methylpyrimidine-5-carboxylate

C

3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-3'-carboxylic acid ethyl ester

3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-3'-carboxylic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 10%
C 33%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Benzylamino-but-2-enoic acid ethyl ester; hydrochloride

(E)-3-Benzylamino-but-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-methylpyrimidine-5-carboxylate
110960-73-1

ethyl 4-methylpyrimidine-5-carboxylate

C

4-Benzylamino-nicotinic acid ethyl ester

4-Benzylamino-nicotinic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 6%
C 33%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Methylamino-pent-2-enoic acid ethyl ester; hydrochloride

(E)-3-Methylamino-pent-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-ethylpyrimidine-5-carboxylate

ethyl 4-ethylpyrimidine-5-carboxylate

C

5-Methyl-4-methylamino-nicotinic acid ethyl ester

5-Methyl-4-methylamino-nicotinic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 5%
C 31%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Dimethylamino-but-2-enoic acid ethyl ester; hydrochloride

(E)-3-Dimethylamino-but-2-enoic acid ethyl ester; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

ethyl 4-methylpyrimidine-5-carboxylate
110960-73-1

ethyl 4-methylpyrimidine-5-carboxylate

C

4-Dimethylamino-nicotinic acid ethyl ester

4-Dimethylamino-nicotinic acid ethyl ester

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 6%
C 30%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

(E)-3-Methylamino-but-2-enoic acid dimethylamide; hydrochloride

(E)-3-Methylamino-but-2-enoic acid dimethylamide; hydrochloride

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

N,N-Dimethyl-4-methylamino-nicotinamide

N,N-Dimethyl-4-methylamino-nicotinamide

C

4-Methyl-pyrimidine-5-carboxylic acid dimethylamide

4-Methyl-pyrimidine-5-carboxylic acid dimethylamide

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;A n/a
B 28%
C 7%
1,3,5-Triazine
290-87-9

1,3,5-Triazine

trichloroacetamidine hydrochloride
42563-97-3

trichloroacetamidine hydrochloride

acetonitrile
75-05-8

acetonitrile

A

2-trichloromethyl-[1,3,5]triazine
30361-83-2

2-trichloromethyl-[1,3,5]triazine

B

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

ethanol
64-17-5

ethanol

chloromethylene-formamidine
4483-79-8

chloromethylene-formamidine

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

Conditions
ConditionsYield
in der Kaelte;
thiourea
17356-08-0

thiourea

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

Conditions
ConditionsYield
With ammonium chloride bei folgendem Kochen mit Raney-Nickel in absol. Aethanol;
1,3,5-Triazine
290-87-9

1,3,5-Triazine

ethanol
64-17-5

ethanol

ammonium chloride

ammonium chloride

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

1,3,5-Triazine
290-87-9

1,3,5-Triazine

hydrogenchloride
7647-01-0

hydrogenchloride

ethanol
64-17-5

ethanol

A

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

B

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

ethanol
64-17-5

ethanol

ammonium chloride

ammonium chloride

thiourea
17356-08-0

thiourea

Raney nickel

Raney nickel

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

formiminoethyl ether

formiminoethyl ether

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

Conditions
ConditionsYield
With ammonia
formamidine acetic acid
3473-63-0

formamidine acetic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

Conditions
ConditionsYield
With acetyl chloride In methanol at 5℃; Inert atmosphere;
With hydrogenchloride In water
With hydrogenchloride In water at 20℃; for 2h;
With hydrogenchloride
triethyl 1,1,2-ethanetricarboxylate
7459-46-3

triethyl 1,1,2-ethanetricarboxylate

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

(4,6-dihydroxy-pyrimidin-5-yl)-acetic acid methyl ester

(4,6-dihydroxy-pyrimidin-5-yl)-acetic acid methyl ester

Conditions
ConditionsYield
Stage #1: triethyl 1,1,2-ethanetricarboxylate; formamidine hydrochloride With sodium methylate In methanol at 20℃;
Stage #2: With hydrogenchloride In methanol; water at 0℃;
99.99%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

nitrosoformamidine

nitrosoformamidine

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite at 0 - 20℃; for 2h;99.2%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

4-carbamoylbenzamidine hydrochloride
59855-11-7

4-carbamoylbenzamidine hydrochloride

2,4-bis<(4-carbamoyl)phenyl>-1,3,5-triazine
156732-82-0

2,4-bis<(4-carbamoyl)phenyl>-1,3,5-triazine

Conditions
ConditionsYield
at 190℃; for 16h;98%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
14152-97-7

2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate

N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-N'-formamidinothiocarboxamides
73556-39-5

N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-N'-formamidinothiocarboxamides

Conditions
ConditionsYield
With triethylamine In acetonitrile Ambient temperature;97%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

ethyl 4,4,4-trifluoroacetoacetate
372-31-6

ethyl 4,4,4-trifluoroacetoacetate

4-hydroxy-6-trifluoromethylpyrimidine
1546-78-7

4-hydroxy-6-trifluoromethylpyrimidine

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In ethanol at 70 - 80℃;96%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

Formamidine; compound with GENERIC INORGANIC NEUTRAL COMPONENT

Formamidine; compound with GENERIC INORGANIC NEUTRAL COMPONENT

Conditions
ConditionsYield
With silver(I) dinitramide In ethanol95%
C14H16N2O7S

C14H16N2O7S

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

C14H13N3O5S

C14H13N3O5S

Conditions
ConditionsYield
Stage #1: formamidine hydrochloride With sodium In 1,4-dioxane at 0℃; for 0.5h; Inert atmosphere;
Stage #2: C14H16N2O7S In 1,4-dioxane
95%
2-Iodobenzoic acid
88-67-5

2-Iodobenzoic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

4-Hydroxyquinazoline
491-36-1

4-Hydroxyquinazoline

Conditions
ConditionsYield
With copper 8-hydroxyquinolinate; sodium hydroxide In water at 100℃; for 0.5h; Microwave irradiation;94%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

2,3,4-tri-O-acetyl-α-D-arabinopyranosyl isotyhiocyanate
62414-75-9

2,3,4-tri-O-acetyl-α-D-arabinopyranosyl isotyhiocyanate

N-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)-N'-formamidinothiocarboxamides
73556-40-8

N-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)-N'-formamidinothiocarboxamides

Conditions
ConditionsYield
With triethylamine In acetonitrile Ambient temperature;93%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

(E)-2-benzyloxy-3-hydroxybut-2-enedioic acid 4-tert-butyl ester 1-methyl ester

(E)-2-benzyloxy-3-hydroxybut-2-enedioic acid 4-tert-butyl ester 1-methyl ester

5-benzyloxy-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid tert-butyl ester

5-benzyloxy-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With sodium methylate In methanol at 20℃; for 24h;93%
C12H15NO3S

C12H15NO3S

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

4-Methyl-5-(4-methylphenyl)pyrimidine

4-Methyl-5-(4-methylphenyl)pyrimidine

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 140℃; for 48h; Inert atmosphere;93%
2-iodo-5-nitro-benzoic acid
19230-50-3

2-iodo-5-nitro-benzoic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-nitroquinazolone
6943-17-5

6-nitroquinazolone

Conditions
ConditionsYield
With 8-quinolinol; sodium hydroxide; copper dichloride In water at 20℃; for 0.333333h; Sealed tube; Microwave irradiation;93%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

2-(4-bromophenyl)-malonic acid dimethyl ester
149506-35-4

2-(4-bromophenyl)-malonic acid dimethyl ester

5-(4-bromophenyl)-4,6-dihydroxypyrimidine
706811-25-8

5-(4-bromophenyl)-4,6-dihydroxypyrimidine

Conditions
ConditionsYield
at 25℃; for 16h; Temperature;92.6%
Stage #1: 2-(4-bromophenyl)-malonic acid dimethyl ester With sodium In methanol at 0 - 20℃; for 18h;
Stage #2: formamidine hydrochloride In methanol at 20℃; for 4h;
91%
Stage #1: 2-(4-bromophenyl)-malonic acid dimethyl ester With sodium methylate In methanol at 0℃; for 18h;
Stage #2: formamidine hydrochloride In methanol at 20℃; for 4h;
Stage #1: 2-(4-bromophenyl)-malonic acid dimethyl ester With sodium In methanol at 0 - 20℃; for 18h;
Stage #2: formamidine hydrochloride In methanol at 20℃; for 4h;
Stage #3: With citric acid In water
Stage #1: 2-(4-bromophenyl)-malonic acid dimethyl ester With sodium In methanol at 0 - 20℃; for 18h;
Stage #2: formamidine hydrochloride In methanol at 20℃; for 4h;
Stage #3: With citric acid In water for 0.166667h;
2-iodoyl-5-methylbenzoic acid
52548-14-8

2-iodoyl-5-methylbenzoic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-methyl-3H-quinazolin-4-one
19181-53-4

6-methyl-3H-quinazolin-4-one

Conditions
ConditionsYield
With copper 8-hydroxyquinolinate; sodium hydroxide In water at 100℃; for 0.5h; Microwave irradiation;92%
C14H11ClO4

C14H11ClO4

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

ethyl 2-(9-chloro-5H-chromeno[4,3-d]pyrimidin-5-yl)acetate

ethyl 2-(9-chloro-5H-chromeno[4,3-d]pyrimidin-5-yl)acetate

Conditions
ConditionsYield
Stage #1: formamidine hydrochloride With base In ethanol for 0.166667h;
Stage #2: C14H11ClO4 In ethanol at 20℃; for 4h;
92%
N-[3-chloro-4-(3-fluorobenzyloxy)phenyl]-2-bromo-5-cyanobenzamide

N-[3-chloro-4-(3-fluorobenzyloxy)phenyl]-2-bromo-5-cyanobenzamide

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-cyano-4-[3-chloro-4-(3-fluorobenzyloxy)phenyl]aminoquinazoline

6-cyano-4-[3-chloro-4-(3-fluorobenzyloxy)phenyl]aminoquinazoline

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50 - 110℃; for 10h;91.7%
N-(5-benzoyl-6-methyl-2-oxo-2H-pyran-3-yl)benzamide
127143-19-5

N-(5-benzoyl-6-methyl-2-oxo-2H-pyran-3-yl)benzamide

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

(E)-2-(benzoylamino)-3-(4-methyl-6-phenylpyrimidin-5-yl)propenoic acid
1192144-38-9

(E)-2-(benzoylamino)-3-(4-methyl-6-phenylpyrimidin-5-yl)propenoic acid

Conditions
ConditionsYield
Stage #1: N-(5-benzoyl-6-methyl-2-oxo-2H-pyran-3-yl)benzamide; formamidine hydrochloride With sodium carbonate In ethanol at 115℃; for 1.5h; Microwave irradiation;
Stage #2: With hydrogenchloride In water pH=2;
91%
formamidine hydrochloride
6313-33-3

formamidine hydrochloride

ethyl 1-tert-butoxycarbonyl-3-oxopiperidine-4-carboxylate
71233-25-5

ethyl 1-tert-butoxycarbonyl-3-oxopiperidine-4-carboxylate

4-hydroxy-5,8-dihydro-6H-pyrido[3,4-d]pyrimidine-7-carboxylic acid tert-butyl ester
1142188-60-0

4-hydroxy-5,8-dihydro-6H-pyrido[3,4-d]pyrimidine-7-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With ethanol; sodium at 20 - 75℃; Temperature; Inert atmosphere;91%
With sodium ethanolate In ethanol Reflux; Inert atmosphere;53%
With sodium ethanolate In ethanol at 70℃; for 5h;42%
5-bromo-2-iodo-benzoic acid
21740-00-1

5-bromo-2-iodo-benzoic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-bromoquinazolin-4(3H)-one
32084-59-6

6-bromoquinazolin-4(3H)-one

Conditions
ConditionsYield
With 8-quinolinol; sodium hydroxide; copper dichloride In water at 20℃; for 0.333333h; Sealed tube; Microwave irradiation; chemoselective reaction;91%
1,1-dichloro-2-cyano-4-methoxy-1,3-butadiene

1,1-dichloro-2-cyano-4-methoxy-1,3-butadiene

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

4-chloro-1H-pyrrolo[2,3-d]pyrimidine
3680-69-1

4-chloro-1H-pyrrolo[2,3-d]pyrimidine

Conditions
ConditionsYield
With sodium methylate In methanol at 25 - 70℃; for 10h;91%
2-bromo-4,5-dimethoxybenzonitrile
109305-98-8

2-bromo-4,5-dimethoxybenzonitrile

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

4-amino-6,7 dimethoxyquinazoline
21575-13-3

4-amino-6,7 dimethoxyquinazoline

Conditions
ConditionsYield
Stage #1: 2-bromo-4,5-dimethoxybenzonitrile; formamidine hydrochloride With potassium carbonate; N,N`-dimethylethylenediamine In 1,4-dioxane for 0.166667h; Inert atmosphere;
Stage #2: With copper(l) iodide In 1,4-dioxane for 2.5h; Solvent; Reagent/catalyst; Inert atmosphere; Reflux;
90.6%
C13H22N4(2+)*2ClO4(1-)

C13H22N4(2+)*2ClO4(1-)

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

N-[(5-pyrimidinyl)methyl]-2-pyridinamine
1383916-51-5

N-[(5-pyrimidinyl)methyl]-2-pyridinamine

Conditions
ConditionsYield
With sodium carbonate In acetonitrile at 60℃; for 35h; Temperature; Reagent/catalyst; Solvent;90.5%
N-[4-(thiazol-2-yl)methoxy-3-chlorophenyl]-2-chloro-5-nitrobenzamide

N-[4-(thiazol-2-yl)methoxy-3-chlorophenyl]-2-chloro-5-nitrobenzamide

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

N-(3-chloro-4-(thiazol-2-ylmethoxy)phenyl)-6-nitroquinazolin-4-amine
1630042-67-9

N-(3-chloro-4-(thiazol-2-ylmethoxy)phenyl)-6-nitroquinazolin-4-amine

Conditions
ConditionsYield
With sodium methylate In methanol; N,N-dimethyl-formamide at 50 - 110℃; for 10h; Temperature;90.2%
N-(5-acetyl-6-methyl-2-oxo-2H-pyran-3-yl)-benzamide
93945-84-7

N-(5-acetyl-6-methyl-2-oxo-2H-pyran-3-yl)-benzamide

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

(E)-2-(benzoylamino)-3-(4,6-dimethylpyrimidin-5-yl)propenoic acid
1192144-33-4

(E)-2-(benzoylamino)-3-(4,6-dimethylpyrimidin-5-yl)propenoic acid

Conditions
ConditionsYield
Stage #1: N-(5-acetyl-6-methyl-2-oxo-2H-pyran-3-yl)-benzamide; formamidine hydrochloride With sodium carbonate In ethanol at 100℃; for 1h; Microwave irradiation;
Stage #2: With hydrogenchloride In water pH=2;
90%
methanol
67-56-1

methanol

triethyl 1,1,2-ethanetricarboxylate
7459-46-3

triethyl 1,1,2-ethanetricarboxylate

sodium methylate
124-41-4

sodium methylate

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

(4,6-dihydroxy-pyrimidin-5-yl)-acetic acid methyl ester

(4,6-dihydroxy-pyrimidin-5-yl)-acetic acid methyl ester

Conditions
ConditionsYield
Stage #1: formamidine hydrochloride With methanol; sodium at 20℃; for 1h;
Stage #2: methanol; triethyl 1,1,2-ethanetricarboxylate; sodium methylate at 20℃; Inert atmosphere;
Stage #3: With hydrogenchloride In water pH=1 - 2; Cooling with ice;
90%
(2-propenyl)propanedioic acid diethyl ester
2049-80-1

(2-propenyl)propanedioic acid diethyl ester

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-hydroxy-5-(2-propen-1-yl)-4(1H)-pyrimidinone
16019-30-0

6-hydroxy-5-(2-propen-1-yl)-4(1H)-pyrimidinone

Conditions
ConditionsYield
Stage #1: formamidine hydrochloride With sodium methylate In methanol at 20℃; for 1h;
Stage #2: (2-propenyl)propanedioic acid diethyl ester In methanol at 20℃; for 36h;
90%
With sodium methylate In methanol at 20℃; for 37h; Inert atmosphere;90%
ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate
39514-19-7

ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

7-benzyl-4-carbonyl-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine

7-benzyl-4-carbonyl-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine

Conditions
ConditionsYield
With potassium hydride; acetic acid In methanol at 20℃; for 0.5h;90%
2-iodo-5-methoxybenzoic acid
54413-93-3

2-iodo-5-methoxybenzoic acid

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

6-Methoxyquinazolin-4-one
19181-64-7

6-Methoxyquinazolin-4-one

Conditions
ConditionsYield
With 8-quinolinol; sodium hydroxide; copper dichloride In water at 20℃; for 0.333333h; Sealed tube; Microwave irradiation;89%
4-<(diethylphosphoryl)oxy>-1,1,1,2,2,3-hexafluoro-3-decene
113138-45-7

4-<(diethylphosphoryl)oxy>-1,1,1,2,2,3-hexafluoro-3-decene

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

5-Fluoro-4-hexyl-6-trifluoromethyl-pyrimidine
117482-32-3

5-Fluoro-4-hexyl-6-trifluoromethyl-pyrimidine

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran Ambient temperature;88%
ethyl 2-methyl-4,4,4-trifluoroacetoacetate
344-00-3

ethyl 2-methyl-4,4,4-trifluoroacetoacetate

formamidine hydrochloride
6313-33-3

formamidine hydrochloride

5-methyl-6-(trifluoromethyl)pyrimidin-4(3H)-one

5-methyl-6-(trifluoromethyl)pyrimidin-4(3H)-one

Conditions
ConditionsYield
Stage #1: ethyl 2-methyl-4,4,4-trifluoroacetoacetate; formamidine hydrochloride In ethanol at 20℃; for 2h;
Stage #2: With sodium ethanolate In ethanol at 80℃; for 4h;
88%

6313-33-3Relevant articles and documents

Syntheses, Crystal Structures, and Optical Properties of the Hexagonal Perovskites Variants ABX3 (B = Ni, A = Gu, FA, MA, X = Cl, Br; B = Mn, A = MA, X = Br)

Daub, Michael,Ketterer, Ines,Hillebrecht, Harald

, p. 280 - 287 (2018/02/09)

Herein we report on our systematic investigations on the solution processed synthesis and characterization of transition metal halides (guanidinium, formamidinium, and methylammonium nickel bromides and chlorides as well as methylammonium manganese bromide) with the composition ABX3 (A = organic cation; B = Mn, Ni; X = Cl, Br). The investigations were carried out with respect to possible applications of 3d transition metal compounds for the perovskite solar cell. All the compounds represent different variants of the hexagonal perovskite structure (2H). Crystal structures and symmetry relations are discussed. Additionally, (CH3NH3)2MnI4, which consists of tetrahedral coordinated Mn2+, and the water containing compounds (CH3NH3)MnBr3·2H2O, which forms chains of edge sharing octahedra, as well as (CH3NH3)NiCl3·2H2O, which consists of dimers of octahedra, are presented. Investigations on the crystal structures are supported by vibrational and optical spectroscopy.

Reentrant Structural and Optical Properties and Large Positive Thermal Expansion in Perovskite Formamidinium Lead Iodide

Fabini, Douglas H.,Stoumpos, Constantinos C.,Laurita, Geneva,Kaltzoglou, Andreas,Kontos, Athanassios G.,Falaras, Polycarpos,Kanatzidis, Mercouri G.,Seshadri, Ram

, p. 15392 - 15396 (2016/12/06)

The structure of the hybrid perovskite HC(NH2)2PbI3(formamidinium lead iodide) reflects competing interactions associated with molecular motion, hydrogen bonding tendencies, thermally activated soft octahedral rotations, and the propensity for the Pb2+lone pair to express its stereochemistry. High-resolution synchrotron X-ray powder diffraction reveals a continuous transition from the cubic α-phase (Pm3m, #221) to a tetragonal β-phase (P4/mbm, #127) at around 285 K, followed by a first-order transition to a tetragonal γ-phase (retaining P4/mbm, #127) at 140 K. An unusual reentrant pseudosymmetry in the β-to-γ phase transition is seen that is also reflected in the photoluminescence. Around room temperature, the coefficient of volumetric thermal expansion is among the largest for any extended crystalline solid.

Novel transition metal complexes with diaminocarbene ligands and their use in reactions catalyzed by transition metals

-

, (2008/06/13)

The invention relates to novel transition metal complexes containing at least one diaminocarbene ligand, to processes for preparing these transition metal complexes and to their use as catalysts in organic reactions.

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