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ChemicalBook--->CAS DataBase List--->26189-59-3

26189-59-3

26189-59-3 Structure

26189-59-3 Structure
IdentificationBack Directory
[Name]

1-Chloro-N,N,2-trimethylpropenylamine
[CAS]

26189-59-3
[Synonyms]

Ghosez′s reagent
TETRAMETHYL-ALPHA-CHLORENAMINE
1-CHLORO-N,N,2-TRIMETHYLPROPENYLAMINE
(1-CHLORO-2-METHYLPROPENYL)DIMETHYLAMINE
1-CHLORO-N,N,2-TRIMETHYL-1-PROPENYLAMINE
1-chloro-N,N,2-trimethyl-1-Propen-1-amine
1-Chloro-N,N,2-trimethylpropenylamine ,98%
1-Chloro-N,N,2-triMethyl-1-propenylaMine 96%
1-Chloro-N,N,2-trimethylpropenylamine, 98.5+%
1-Chloro-N,N,2-triMethylpropenylaMine, 98.5+% 5ML
[Molecular Formula]

C6H12ClN
[MDL Number]

MFCD00800562
[MOL File]

26189-59-3.mol
[Molecular Weight]

133.62
Chemical PropertiesBack Directory
[Appearance]

Colorless to yellow liquid
[Boiling point ]

129-130 °C(lit.)
[density ]

1.01 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.453(lit.)
[Fp ]

80 °F
[storage temp. ]

Freezer (-20°C)
[form ]

Liquid
[pka]

4.27±0.70(Predicted)
[color ]

Colorless to yellow
Hazard InformationBack Directory
[Chemical Properties]

Colorless to yellow liquid
[Uses]

1-Chloro-N,N,2-trimethyl-1-propenylamine is an acid halogenation reagent developed by Ghosez, that enables the conversion of carboxylic acids into the corresponding chlorides under strictly neutral conditions. This method was successfully used in the total synthesis of caloporoside, roseophilin, (-)-enniatin B, (±)-epimeloscine and (±)-meloscine.
[Synthesis Reference(s)]

Journal of the American Chemical Society, 94, p. 2869, 1972 DOI: 10.1021/ja00763a061
Organic Syntheses, Coll. Vol. 6, p. 282, 1988
Tetrahedron Letters, 25, p. 5043, 1984 DOI: 10.1016/S0040-4039(01)91114-1
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

10-34
[Safety Statements ]

16-26-36/37/39-45
[RIDADR ]

UN 2734 8/PG 1
[WGK Germany ]

3
[HS Code ]

29211990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Dichloromethane-->N,N-Dimethylformamide-->PETROLEUM ETHER-->Phosphorus oxychloride-->Magnesium sulfate-->Triethylamine-->Sodium bicarbonate-->Dimethylamine-->Isobutyryl chloride
[Preparation Products]

Methyl 1,2,3-benzothiadiazole-7-carboxylate
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