tris hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In methanol for 1h; Heating; | 80% |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 20℃; for 3h; |
1,4-dithiane-2,5-diol
tris hydrochloride
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 3h; Reflux; | 97% |
Conditions | Yield |
---|---|
Stage #1: cycloxexanone dimethyl ketal; tris hydrochloride With toluene-4-sulfonic acid In N,N-dimethyl-formamide for 17h; Stage #2: With triethylamine In ethyl acetate | 94% |
benzaldehyde dimethyl acetal
tris hydrochloride
5-amino-5-hydroxymethyl-2-phenyl-1,3-dioxane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid; triethylamine for 12h; Ambient temperature; | 90% |
Conditions | Yield |
---|---|
Stage #1: 3H3N*3H(1+)*[CrMo6O18(OH)6](3-); 2-amino-2-hydroxymethyl-1,3-propanediol In water at 130℃; for 13h; Stage #2: tris hydrochloride In water at 20℃; for 0.166667h; | 90% |
tris hydrochloride
2,2-dimethoxy-propane
(5-amino-2,2-dimethyl-1,3-dioxan-5-yl)methanol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid; N,N-dimethyl-formamide for 12h; Ambient temperature; | 86% |
Stage #1: tris hydrochloride; 2,2-dimethoxy-propane With toluene-4-sulfonic acid In N,N-dimethyl-formamide at 20℃; for 60h; Stage #2: With triethylamine In methanol; N,N-dimethyl-formamide Sonication; Stage #3: With triethylamine In methanol; ethyl acetate; N,N-dimethyl-formamide at 20℃; for 0.166667h; | 86% |
Stage #1: tris hydrochloride; 2,2-dimethoxy-propane; toluene-4-sulfonic acid In N,N-dimethyl-formamide at 20℃; for 18h; Stage #2: With triethylamine In ethyl acetate for 0.5h; | 85% |
tris hydrochloride
β-naphthaldehyde
5-amino-5-hydroxymethyl-2-(2-naphthyl)-1,3-dioxane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 12h; Condensation; Heating; | 85% |
tris hydrochloride
1-naphthaldehyde
5-amino-5-hydroxymethyl-2-(1-naphthyl)-1,3-dioxane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 12h; Condensation; Heating; | 82% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In 1,4-dioxane; water at 20℃; for 19h; | 80% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de; | 77% |
cycloxexanone dimethyl ketal
tris hydrochloride
3-amino-3-(hydroxymethyl)-1,5-dioxaspiro[5.5]undecane
Conditions | Yield |
---|---|
Stage #1: cycloxexanone dimethyl ketal; tris hydrochloride With toluene-4-sulfonic acid In N,N-dimethyl-formamide at 21 - 23℃; for 18h; Inert atmosphere; Sealed tube; Stage #2: With triethylamine In ethyl acetate for 12h; | 74% |
Conditions | Yield |
---|---|
at 140℃; for 30h; | 70% |
tris hydrochloride
3'-tert-butyldimethylsilylthymidine 5'-carboxaldehyde
Conditions | Yield |
---|---|
With triethylammonium bicarbonate buffer In acetonitrile at 20℃; pH=8; | 67% |
tris hydrochloride
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide for 2h; | 67% |
Conditions | Yield |
---|---|
In methanol; water at 60℃; for 1h; | 58% |
carbon disulfide
tris hydrochloride
A
4,4-bis(hydroxymethyl)thiazolidine-2-thione
B
4,4-bis(hydroxymethyl)oxazolidine-2-thione
C
4-hydroxymethyl-4-thiomethyl-thiazolidine-2-thione
Conditions | Yield |
---|---|
With sodium hydroxide In water at 60℃; for 24h; | A 45% B 18% C 11% |
tris hydrochloride
3,4-dichlorobenzaldehyde
B
2,8-di-(3,4-dichlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de; | A n/a B n/a C 35% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de; | 34% |
N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-isocyanatoheptanediamide
tris hydrochloride
trifluoroacetic acid
N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-(3-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)ureido)heptanediamide
Conditions | Yield |
---|---|
Stage #1: N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-isocyanatoheptanediamide; tris hydrochloride With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h; Stage #2: trifluoroacetic acid In water; N,N-dimethyl-formamide | 26% |
tris hydrochloride
4-bromo-benzaldehyde
B
2,8-di-(m-bromophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane
C
{bis-(2,8-di-(m-bromophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]-octane 5-methoxy)methyl}-3-bromobenzene
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de; | A n/a B n/a C 25% |
4-Trifluoromethylbenzaldehyde
tris hydrochloride
C
{bis(2,8-di-(p-trifluoromethylphenyl)-1-aza-3,7-dioxabicyclo-[3.3.0]octane 5-methoxy)methyl}-4-trifluoromethylbenzene
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de; | A n/a B n/a C 13% |
2-benzoyloxyacetyl chloride
tris hydrochloride
Benzoic acid (2-hydroxy-1,1-bis-hydroxymethyl-ethylcarbamoyl)-methyl ester
Conditions | Yield |
---|---|
In benzene Ambient temperature; |
tris hydrochloride
N,N'-dimethyl-N'-(p-nitrophenyl)-N-nitrosourea
B
N-methyl(p-nitroaniline)
Conditions | Yield |
---|---|
With water; sodium chloride; cetyltrimethylammonim bromide at 24.8℃; Rate constant; micellar effect investigated at pH 8.05; |
myo-inositol-1,2-cyclic phosphate
tris hydrochloride
Conditions | Yield |
---|---|
With glycerol In water bacterial phosphatidylinositol-specific phospholipase C presence; |
tris hydrochloride
Conditions | Yield |
---|---|
With mesotetrakis(4-N-methylpiridiniumyl)porphyrinatomanganeseIII; oxygen; tris hydrochloride; sodium sulfite at 4℃; for 5h; pH=9; Product distribution; Enzymatic reaction; |
Conditions | Yield |
---|---|
With mesotetrakis(4-N-methylpiridiniumyl)porphyrinatomanganeseIII; oxygen; tris hydrochloride; sodium sulfite at 20℃; for 1h; pH=9; Product distribution; Enzymatic reaction; |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 16h; |
Molecular Structure:
Molecular Formula: C4H12ClNO3
Molecular Weight: 157.596
IUPAC Name: 2-Amino-2-(hydroxymethyl)propane-1,3-diol hydrochloride
Synonyms of Tris hydrochloride (CAS NO.1185-53-1): 2-Amino-2-hydroxymethyl-1,3-propanediol hydrochloride ; EINECS 214-684-5 ; Tris chloride ; Tris hydrochloride buffer ; Tris(hydroxymethyl)aminomethane hydrochloride ; Trizma hydrochloride ; Tromethamine HCl ; Tris(hydroxymethyl)aminomethanehydrochloride ; UNII-383V75M34E ; 1,3-Propanediol, 2-amino-2-(hydroxymethyl)-, hydrochloride ; 1,3-Propanediol, 2-amino-2-(hydroxymethyl)-, hydrochloride (1:1)
CAS NO: 1185-53-1
Product Categories: Buffer
Melting Point: 150-152 °C
H bond acceptors: 4
H bond donors: 5
Freely Rotating Bonds: 7
Polar Surface Area: 30.93 Å2
Flash Point: 169.7 °C
Enthalpy of Vaporization: 69.73 kJ/mol
Boiling Point: 357 °C at 760 mmHg
Vapour Pressure: 1.57E-06 mmHg at 25°C
Tris hydrochloride (CAS NO.1185-53-1) is used as a organic intermediate.
Safety Information of Tris hydrochloride (CAS NO.1185-53-1):
Hazard Codes:Xi
Risk Statements:36/37/38
36/37/38:Irritating to eyes, respiratory system and skin
Safety Statements:26-36
26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36:Wear suitable protective clothing
WGK Germany:3
F:3
HS Code:29221980
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