Conditions | Yield |
---|---|
With thionyl chloride In chloroform at 0 - 20℃; for 1h; Reflux; | 95% |
With thionyl chloride In chloroform | 95% |
With thionyl chloride In chloroform Reflux; Cooling with ice; |
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride at 60℃; for 24h; |
(2-chloropropyl)dimethylamine hydrochloride
6,7-methylenedioxyquinoline-4-carboxylic acid N-(2-iodo-4,5-dimethoxyphenyl)amide
Conditions | Yield |
---|---|
With sodium hydride; sodium iodide In N,N-dimethyl-formamide at 65℃; for 3h; | 89% |
Conditions | Yield |
---|---|
With sodium hydroxide In water | 82% |
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 6h; Reflux; | 80% |
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With sodium azide In water at 80℃; | 80% |
1-(3-(4-hydroxyphenyl)-7-methoxy-3,3a,4,5-tetrahydro-2H-benzo[g]indazol-2-yl)ethanone
(2-chloropropyl)dimethylamine hydrochloride
C25H31N3O3
Conditions | Yield |
---|---|
With potassium carbonate In chloroform; acetone at 80℃; | 75% |
8-methoxy-4-(4-hydroxyphenyl)-5,6-dihydrobenzo[h]quinazolin-2-amine
(2-chloropropyl)dimethylamine hydrochloride
4-(4-(1-(dimethylamino)propan-2-yloxy)phenyl)-5,6-dihydro-8-methoxybenzo[h]quinazolin-2-amine
Conditions | Yield |
---|---|
With potassium carbonate In chloroform; acetone at 80℃; | 75% |
With potassium carbonate In chloroform; acetone at 80℃; | 75% |
(2-chloropropyl)dimethylamine hydrochloride
1-(5-cyano-2-mercaptobenzenesulphonyl)-2-imidazolidinone
Conditions | Yield |
---|---|
With sodium isopropylate In isopropyl alcohol for 16h; Heating; | 65% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 80℃; | 63% |
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With sodium isopropylate In isopropyl alcohol for 16h; Heating; | 57% |
(2-chloropropyl)dimethylamine hydrochloride
1-(4-chloro-5-cyano-2-mercaptobenzenesulphonyl)-2-imidazolidinone
Conditions | Yield |
---|---|
With sodium isopropylate In isopropyl alcohol for 16h; Heating; | 50% |
(2-chloropropyl)dimethylamine hydrochloride
2-methyl-10H-pyrimido<1,2-a>benzimidazol-4-one
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 30h; Heating; | 43% |
3-hydroxybenzo[b]naphtho[2,3-d]furane-6,11-dione
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In chloroform; water Heating; | 32.7% |
7-chloro-8-hydroxybenzo[4,5]furo[3,2-g]quinoline-5,11-dione
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In chloroform; water Heating; | 31% |
(2-chloropropyl)dimethylamine hydrochloride
2-chloro-3-hydroxybenzo[b]naphtho[2,3-d]furan-6,11-dione
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In chloroform; water Heating; | 25.9% |
2-(4-propoxyphenyl)-4-hydroxyquinoline
(2-chloropropyl)dimethylamine hydrochloride
N,N-dimethyl-2-{[2-(4-propoxyphenyl)quinolin-4-yl]oxy}propan-1-amine hydrochloride
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 70℃; Inert atmosphere; | 18% |
(2-chloropropyl)dimethylamine hydrochloride
1,3-dihydroxybenzo[b]naphtho[2,3-d]furan-6,11-dione
3-[2-(dimethylamino)isopropoxy]-1-hydroxybenzo[b]naphtho[2,3-d]furan-6,11-dione
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In chloroform; water at 20℃; Reflux; | 16% |
8-hydroxybenzo[4,5]furo[3,2-g]quinoline-5,11-dione
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In chloroform; water Heating; | 15.7% |
10H-phenothiazine
(2-chloropropyl)dimethylamine hydrochloride
isopromethazine
Conditions | Yield |
---|---|
With potassium hydroxide; Aliquat 336 at 80℃; for 1h; | 12% |
N-benzhydrylpyrimidin-2-amine
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With lithium amide; benzene |
sodium methylate
(2-chloropropyl)dimethylamine hydrochloride
A
(β-methoxy-isopropyl)-dimethyl-amine
B
(2-methoxy-propyl)-dimethyl-amine
Conditions | Yield |
---|---|
With methanol |
N-[tricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,9,12,14-heptaen-2-ylidene]hydroxylamine
(2-chloropropyl)dimethylamine hydrochloride
Conditions | Yield |
---|---|
With sodium methylate In methanol Heating; |
(2-chloropropyl)dimethylamine hydrochloride
3-<2-Dimethylamino-1-methyl-aethyl>-thiophosphorsaeure
Conditions | Yield |
---|---|
With lithium thiophosphate powder |
(2-chloropropyl)dimethylamine hydrochloride
5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one
3-(2-dimethylamino-1-methyl-ethyl)-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one
Conditions | Yield |
---|---|
(i) NaH, dioxane, (ii) /BRN= 3670215/; Multistep reaction; |
Benzophenone oxime
(2-chloropropyl)dimethylamine hydrochloride
methyl iodide
Conditions | Yield |
---|---|
(i) NaOMe, MeOH, (ii) /BRN= 969135/, acetone; Multistep reaction; |
Benzophenone oxime
(2-chloropropyl)dimethylamine hydrochloride
methyl iodide
Conditions | Yield |
---|---|
(i) NaOMe, MeOH, (ii) /BRN= 969135/, acetone; Multistep reaction; |
N-[cyclohexyl(phenyl)methylidene]hydroxylamine
(2-chloropropyl)dimethylamine hydrochloride
methyl iodide
Conditions | Yield |
---|---|
(i) NaOMe, MeOH, (ii) /BRN= 969135/, acetone; Multistep reaction; |
(2-chlorophenyl)phenylmethanone oxime
(2-chloropropyl)dimethylamine hydrochloride
methyl iodide
Conditions | Yield |
---|---|
(i) NaOMe, MeOH, (ii) /BRN= 969135/, acetone; Multistep reaction; |
(2-chlorophenyl)phenylmethanone oxime
(2-chloropropyl)dimethylamine hydrochloride
methyl iodide
Conditions | Yield |
---|---|
(i) NaOMe, MeOH, (ii) /BRN= 969135/, acetone; Multistep reaction; |
N-(2-chloro-3-pyridinyl)acetamide
(2-chloropropyl)dimethylamine hydrochloride
1-(2,4-Dimethyl-3,4-dihydro-2H-pyrido[2,3-b]pyrazin-1-yl)-ethanone
Conditions | Yield |
---|---|
With sodium hydride 1.) DMF, 0 deg C, 10 min, 2.) 80 deg C, 1 h; Yield given. Multistep reaction; |
IUPAC Name: 2-Chloro-N,N-dimethylpropan-1-amine hydrochloride
Synonyms of 1-Propanamine,2-chloro-N,N-dimethyl-, hydrochloride (1:1) (CAS NO.4584-49-0): 2-Chloropropyl)dimethylamine monohydrochloride ; 1-(Dimethylamino)-2-chloropropane hydrochloride ; 1-Methyl-2-dimethylaminoethyl chloride hydrochloride ; 2-(Dimethylamino)-1-methylethyl chloride hydrochloride ; 2-(Dimethylamino)isopropyl chloride hydrochloride ; 2-Chloro-N',N'-dimethylaminopropane hydrochloride ; 2-Chloro-N,N-dimethyl-1-propanamine hydrochloride ; 2-Chloropropyl-dimethylamine hydrochloride ; AI3-26684 ; EINECS 224-971-7 ; N,N-Dimethyl-2-chloropropylamine hydrochloride ; NSC 53532 ; NSC 5367 ; Propane, 1-(N,N-dimethylamino)-2-chloro-, hydrochloride
CAS NO: 4584-49-0
Classification Code: Drug / Therapeutic Agent
Molecular Formula of 1-Propanamine,2-chloro-N,N-dimethyl-, hydrochloride (1:1) (CAS NO.4584-49-0): C5H13Cl2N
Molecular Weight: 158.0694
Molecular Structure:
Melting Point: 187-190 °C
Polar Surface Area: 3.24 Å2
Flash Point of 1-Propanamine,2-chloro-N,N-dimethyl-, hydrochloride (1:1) (CAS NO.4584-49-0): 2.9 °C
Enthalpy of Vaporization: 32.18 kJ/mol
Boiling Point: 81.1 °C at 760 mmHg
Vapour Pressure: 83 mmHg at 25°C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | subcutaneous | 200mg/kg (200mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Journal of Pharmacology and Experimental Therapeutics. Vol. 98, Pg. 121, 1950. |
Hazard Codes: Xn,Xi
Risk Statements: 22-36/37/38
R22: Harmful if swallowed.
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36: Wear suitable protective clothing.
RIDADR: 2811
WGK Germany: 3
RTECS: TY1225000
HazardClass: 6.1(b)
PackingGroup: III
HS Code: 29211980
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