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inquiryAMINOPROPYL DIHYDROGEN PHOSPHATE Application:AMINOPROPYL DIHYDROGEN PHOSPHATE
Supply top quality products with a reasonable price Application:api
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Hangzhou ZeErRui Chemical Co., Ltd. is focused on customization, research and development and production of APIs and advanced intermediates, which can effectively compensate for the deficiencies of traditional CRO and CMO. Priority of high-tech barri
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factory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
N2,N3-didechloroethylifosfamide
A
3-aminopropyl dihydrogen phosphate
B
1-propanol, 3-amino-, hydrogen phosphoramidate
C
2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-ol
Conditions | Yield |
---|---|
With hydrogenchloride for 0.333333h; Ambient temperature; | A n/a B 95% C n/a |
With sodium cacodylate at 25℃; Rate constant; other subst. ifosfamides; var. pH; |
Conditions | Yield |
---|---|
Stage #1: propan-1-ol-3-amine With triethylamine; trichlorophosphate In dichloromethane at 0 - 26℃; for 1h; Inert atmosphere; Stage #2: With hydrogenchloride; water at 0℃; for 2h; Reflux; Stage #3: With triethylamine In water at 18 - 26℃; for 1h; | 38.4% |
With PPA at 180℃; unter vermindertem Druck; | |
With PPA at 180℃; under 18 Torr; |
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With hydrogenchloride In methanol |
Conditions | Yield |
---|---|
With KCl*HCl buffer at 20℃; Product distribution; other buffers, temperature; |
Dechloroethylcyclophosphamide
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With hydrogenchloride for 24h; Ambient temperature; |
Dechloroethylcyclophosphamide
A
3-aminopropyl dihydrogen phosphate
B
(2-chloro-ethyl)-phosphoramidic acid mono-(3-amino-propyl) ester
Conditions | Yield |
---|---|
With hydrogenchloride |
Dechloroethylcyclophosphamide
A
3-aminopropyl dihydrogen phosphate
B
chloroethylamine
C
(2-chloro-ethyl)-phosphoramidic acid mono-(3-amino-propyl) ester
D
2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-ol
Conditions | Yield |
---|---|
With sodium cacodylate at 20℃; Rate constant; other subst. ifosfamides; var. pH; |
N2,N3-didechloroethylifosfamide
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With hydrogenchloride for 10h; Ambient temperature; |
1-propanol, 3-amino-, hydrogen phosphoramidate
A
3-aminopropyl dihydrogen phosphate
B
2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-ol
Conditions | Yield |
---|---|
With sodium cacodylate at 25℃; Rate constant; |
(2-chloro-ethyl)-phosphoramidic acid mono-(3-amino-propyl) ester
A
3-aminopropyl dihydrogen phosphate
B
chloroethylamine
C
2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-ol
Conditions | Yield |
---|---|
With sodium cacodylate at 25℃; Rate constant; |
2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-ol
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With sodium cacodylate at 25℃; Rate constant; |
sesamol, 3-aminopropane phosphoric acid diester
A
Sesamol
B
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With water; alkaline phosphatase pH=7.4; Product distribution / selectivity; Aqueous phosphate buffer; | |
With alkaline phosphatase pH=7.4; Aqueous phosphate buffer; Enzymatic reaction; |
3-aminopropyl dibenzyl phosphate
3-aminopropyl dihydrogen phosphate
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid at 20℃; for 1h; |
3-aminopropyl dihydrogen phosphate
7-{6-[(ethylcarbamoyl)amino]-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}-1-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
3-{[(7-{6-[(ethylcarbamoyl)amino]-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}-1-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-4-oxo-1,4-dihydroquinolin-3-yl)carbonyl]amino}propyl dihydrogen phosphate
Conditions | Yield |
---|---|
Stage #1: 7-{6-[(ethylcarbamoyl)amino]-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}-1-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid With triethylamine; HATU In N,N-dimethyl-formamide at 18 - 26℃; for 0.166667h; Stage #2: 3-aminopropyl dihydrogen phosphate In N,N-dimethyl-formamide at 18 - 26℃; for 2h; | 28.6% |
3-aminopropyl dihydrogen phosphate
3-{[(1-ethyl-7-{6-[(ethylcarbamoyl)amino]-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}-4-oxo-1,4-dihydroquinolin-3-yl)carbonyl]amino}propyl dihydrogen phosphate
Conditions | Yield |
---|---|
Stage #1: 1-ethyl-7-{6-[(ethylcarbamoyl)amino]-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}-4-oxo-1,4-dihydroquinoline-3-carboxylic acid With triethylamine; HATU In N,N-dimethyl-formamide at 18 - 26℃; for 1h; Stage #2: 3-aminopropyl dihydrogen phosphate In N,N-dimethyl-formamide | 22.5% |
3-aminopropyl dihydrogen phosphate
acetic anhydride
phosphoric acid mono-(3-acetylamino-propyl ester)
Conditions | Yield |
---|---|
With pyridine at 60℃; |
3-aminopropyl dihydrogen phosphate
benzoyl chloride
phosphoric acid mono-(3-benzoylamino-propylester); barium salt
Conditions | Yield |
---|---|
With barium dihydroxide |
Conditions | Yield |
---|---|
With diethylamine |
3-aminopropyl dihydrogen phosphate
phenyl isocyanate
3-N-Phenylcarbamylamino-propyl-phosphorsaeuremonoester
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane |
3-aminopropyl dihydrogen phosphate
phenyl isothiocyanate
3-N-Phenylthiocarbamylamino-propyl-phosphorsaeuremonoester
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane |
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