Conditions | Yield |
---|---|
With hydrogenchloride for 24h; Heating; | 99% |
Conditions | Yield |
---|---|
Stage #1: dimethyl amine; chloroacetic acid In water at 25 - 55℃; for 11h; Stage #2: With hydrogenchloride In water at 40℃; |
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water; acetone |
N,N-dimethylglycine hydrochoride
benzylamine
N-benzyl-2-(dimethylamino)acetamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; Inert atmosphere; | 98% |
N,N-dimethylglycine hydrochoride
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 0 - 20℃; | 96% |
Conditions | Yield |
---|---|
With triethylamine; diethyl dicarbonate In dichloromethane at 20℃; for 13h; | 95% |
Conditions | Yield |
---|---|
With pyridine; 2-chloro-1,3-dimethylimidazolinium chloride In dichloromethane at 20℃; for 96h; Esterification; | 92% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethylglycine hydrochoride With triethylamine In dichloromethane; butan-1-ol at 20℃; for 1h; Inert atmosphere; Stage #2: isobutyl chloroformate In dichloromethane; butan-1-ol at -15℃; for 2h; Inert atmosphere; Stage #3: C26H25N3O4S In dichloromethane; butan-1-ol at 20℃; for 19h; Inert atmosphere; | A 91% B 6% |
copper(I) iodide
N,N-dimethylglycine hydrochoride
phenol
1'-pentyl-6-phenoxyspiro[1-benzofuran-3,3'-indol]-2'(1'H)-one
Conditions | Yield |
---|---|
With caesium carbonate In 1,4-dioxane | 87% |
N,N-dimethylglycine hydrochoride
benzyl alcohol
2-(dimethylamino)acetic acid benzyl ester
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap; dicyclohexyl-carbodiimide In dichloromethane at 0℃; Inert atmosphere; | 87% |
(3R,4R)-3,4-bis((9Z,12Z)-octadec-9,12-dienyloxy)pyrrolidine
N,N-dimethylglycine hydrochoride
(3R,4R)-1-(2-(dimethylamino)acetyl)-3,4-bis((9Z,12Z)-octadec-9,12-dienyloxy)pyrrolidine
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In chloroform at 20℃; for 1.5h; | 86.8% |
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In chloroform at 20℃; for 1.5h; | 86.8% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethylglycine hydrochoride With sodium hydroxide In ethanol at 20℃; for 0.5h; Stage #2: n-tetradecanoic acid With calcium hydroxide In ethanol at 20℃; for 4h; | 84.33% |
N,N-dimethylglycine hydrochoride
N,N-dimethylaminoacetyl chloride hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride at 78℃; for 0.5h; | 84% |
With phosphorus pentachloride | 82% |
With oxalyl dichloride In dichloromethane at 20℃; for 2h; |
N,N-dimethylglycine hydrochoride
Conditions | Yield |
---|---|
Stage #1: N,N-dimethylglycine hydrochoride With sodium hydroxide In ethanol at 20℃; for 0.5h; Stage #2: With sulfuric acid; calcium hydroxide In ethanol at -20 - 20℃; for 4h; | 83.67% |
N,N-dimethylglycine hydrochoride
1,8,17,24-tetraoxa-33,34,35,36-tetrakis(hydroxymethyl)<8.8>(1,4)naphthalenophane
1,8,17,24-tetraoxa-33,34,35,36-tetrakis(N,N-dimethylglycyloxymethyl)<8.8>(1,4)naphthalenophane
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In pyridine for 4h; Ambient temperature; | 82% |
N,N-dimethylglycine hydrochoride
Conditions | Yield |
---|---|
Stage #1: C-acridin-4-yl-methylamine; hydrochloride With ammonia In water Stage #2: N,N-dimethylglycine hydrochoride With benzotriazol-1-ol; triethylamine In dichloromethane for 48h; | 80% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In pyridine for 24h; Ambient temperature; | 79% |
3,5-seco-4-nor-cholestane-5-one-3-ol
N,N-dimethylglycine hydrochoride
C30H53NO3
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 16h; | 78% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 16h; | 78% |
dimethylaminoacetic acid
N,N-dimethylglycine hydrochoride
2-(4-{2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}thio)-3,5-dicyano-6-[(N,N-dimethylglycyl)-amino]pyridin-4-yl}phenoxy)ethyl N,N-dimethylglycinate
Conditions | Yield |
---|---|
Stage #1: Capadenoson; N,N-dimethylglycine hydrochoride With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap In dichloromethane Reflux; Stage #2: dimethylaminoacetic acid With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap In dichloromethane Reflux; Stage #3: With sodium hydrogencarbonate In dichloromethane | 78% |
N,N-dimethylglycine hydrochoride
Conditions | Yield |
---|---|
With phosphoric acid; sodium hydroxide; calcium hydroxide In ethanol at 20℃; for 4h; | 77.53% |
N,N-dimethylglycine hydrochoride
2-(N,N-Dimethylglycyl)aminomethyl-5-methyl-2,3,6,7-tetrahydrofuro-[2,3-f]quinoline-7-one.HCl
Conditions | Yield |
---|---|
With benzotriazol-1-ol In N-methyl-acetamide | 77% |
2,5-bis-[5-{2-(N-hydroxyamidino)-pyridyl}]selenophene
N,N-dimethylglycine hydrochoride
2,5-bis-[5-{2-N-(N,N-dimethylaminoacetoxyamidino)-pyridyl}]selenophene
Conditions | Yield |
---|---|
Stage #1: N,N-dimethylglycine hydrochoride With 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 60℃; for 2h; Stage #2: 2,5-bis-[5-{2-(N-hydroxyamidino)-pyridyl}]selenophene In N,N-dimethyl-formamide at 0 - 20℃; for 12h; | 77% |
N,N-dimethylglycine hydrochoride
1,4-bis(propynyloxy)-2,3-bis(hydroxymethyl)naphthalene
1,4-bis(propynyloxy)-2,3-bis(N,N-dimethylglycyloxymethyl)naphthalene
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 5h; Ambient temperature; | 76% |
Gly-OBz
N,N-dimethylglycine hydrochoride
benzyl 2-(2-(dimethylamino)acetamido)acetate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide at 20℃; for 16h; | 76% |
4-acetaminophenol
N,N-dimethylglycine hydrochoride
4-acetamidophenyl 2-(dimethylamino)acetate hydrochloride
Conditions | Yield |
---|---|
With pyridine; dicyclohexyl-carbodiimide at 20℃; | 75% |
Conditions | Yield |
---|---|
Stage #1: C26H25N3O4S; N,N-dimethylglycine hydrochoride In methanol at 0℃; for 1h; Inert atmosphere; Stage #2: With 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride In methanol at 20℃; for 38h; Inert atmosphere; | 75% |
cholesterol
N,N-dimethylglycine hydrochoride
cholesteryl 2-(dimethylamino)acetate
Conditions | Yield |
---|---|
Stage #1: cholesterol; N,N-dimethylglycine hydrochoride With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.0833333h; Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 74.6% |
Stage #1: cholesterol; N,N-dimethylglycine hydrochoride With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.0833333h; Stage #2: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethylglycine hydrochoride With sodium hydroxide In ethanol at 20℃; for 0.5h; Stage #2: toluene-4-sulfonic acid With calcium hydroxide In ethanol at 20℃; for 4h; | 74.23% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 20℃; for 4h; | 73.06% |
N,N-dimethylglycine hydrochoride
acridin-4-ylmethanol
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In acetone at 20℃; for 96h; | 73% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 72% |
5-(2-benzyl-2H-indazol-6-yl)-7-morpholin-2-ylpyrrolo[2,1-f][1,2,4]triazin-4-amine
N,N-dimethylglycine hydrochoride
Conditions | Yield |
---|---|
With 4-methyl-morpholine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate In tetrahydrofuran at 20℃; for 1h; | 71% |
The Molecular formula of N-METHYLSARCOSINE HYDROCHLORIDE (2491-06-7):C4H10ClNO2
The Molecular Weight of N-METHYLSARCOSINE HYDROCHLORIDE (2491-06-7):139.58
The Molecular Structure of N-METHYLSARCOSINE HYDROCHLORIDE (2491-06-7) is:
Density:1.069g/cm3
Melting point:189-194 °C(lit.)
Boiling point:175.2 °C at 760 mmHg
Flash point:59.8 °C
Solubility in water:100 g/L (20 °C
Sensitive:Hygroscopic
Merck:14,3244
BRN:3910578
Enthalpy of Vaporization:45.38 kJ/mol
Vapour Pressure: 0.556 mmHg at 25°C
Appearance:white crystalline powder
IUPAC Name: 2-(dimethylamino)acetic acid hydrochloride
Synonyms: n,n-dimethyl-glycinhydrochloride ; N,N-DIMETHYLAMINOACETIC ACID HYDROCHLORIDE ; N,N-DIMETHYL-GLY-OH HCL ; N,N-DIMETHYLGLYCINE HCL ; N,N-DIMETHYLGLYCINE HYDROCHLORIDE ; DMG HYDROCHLORIDE ; DIMETHYLGLYCINE HCL ; n-methylsarcosinehydrochloride
It is used as a raw material for medicine and health care products.It also used as chemical intermediates for health care products.
1. | orl-rat LD50:3900 mg/kg | JACTDZ Journal of the American College of Toxicology. 1 (1992),198. |
Reported in EPA TSCA Inventory.
Moderately toxic by ingestion. When heated to decomposition it emits toxic vapors of NOx and HCl.
Risk Statements
R36/37/38:Irritating to eyes, respiratory system and skin .
Safety Statements
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
WGK Germany:2
RTECS:MB9995000
Conditions to Avoid: Incompatible materials, strong oxidants.
Chemical Stability:Stable under normal temperatures and pressures.
Incompatibilities with Other Materials: Strong oxidizing agents.
Hazardous Decomposition Products: Hydrogen chloride, nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide, nitrogen.
Hazardous Polymerization: Has not been reported.
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