ChemicalBook--->CAS DataBase List--->3196-23-4

3196-23-4

3196-23-4 Structure

3196-23-4 Structure
IdentificationBack Directory
[Name]

METHYL 1-BROMOCYCLOHEXANECARBOXYLATE
[CAS]

3196-23-4
[Synonyms]

LABOTEST-BB LT00160081
METHYL 1-BROMOCYCLOHEXANECARBOXYLATE
methyl 1-bromocyclohexane-1-carboxylate
Methyl 1-broMocyclohexanecarboxylate 97%
METHYL 1-BROMOCYCLOHEXANECARBOXYLATE, 97 %
1-Bromocyclohexanecarboxylic acid methyl ester
Cyclohexanecarboxylic acid, 1-bromo-, methyl ester
[Molecular Formula]

C8H13BrO2
[MDL Number]

MFCD00134214
[MOL File]

3196-23-4.mol
[Molecular Weight]

221.09
Chemical PropertiesBack Directory
[Boiling point ]

115-116 °C/19 mmHg (lit.)
[density ]

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

n20/D 1.493(lit.)
[Fp ]

222 °F
[storage temp. ]

2-8°C
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

34-36/37
[Safety Statements ]

26-27-28-36/37/39-45
[RIDADR ]

UN 3265 8/PG 2
[WGK Germany ]

3
[HazardClass ]

8
[PackingGroup ]

III
Hazard InformationBack Directory
[Uses]

Methyl 1-bromocyclohexanecarboxylate may be used in the improved method of preparation of methyl 3-oxo-1-cyclohexene-1-carboxylate. It may be used in the Reformatsky synthesis of 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones.
[General Description]

Methyl 1-bromocyclohexanecarboxylate reacts with zinc and substituted chalcones to yield the corresponding spiro-3,4-dihydropyran-2-one derivatives, 3-aryl-5-aryl-2-oxaspiro[5.5]undec-3-en-1-ones. Reformatsky reaction of methyl 1-bromocyclohexanecarboxylate with 2-aryl-2-oxoacetaldehyde is reported. Methyl 1-bromocyclohexanecarboxylate reacts with zinc and amides or methylamides of 3-aryl-2-cyanopropenoic acids to yield 5-aryl-1,3-dioxo-2-azaspiro[5.5]undecane-4-carbonitriles or 5-aryl-2-methyl-1,3-dioxo-2-azaspiro[5.5]undecane-4-carbonitriles.
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 1-BROMOCYCLOHEXANECARBOXYLATE(3196-23-4)1HNMR
METHYL 1-BROMOCYCLOHEXANECARBOXYLATE(3196-23-4)IR
METHYL 1-BROMOCYCLOHEXANECARBOXYLATE(3196-23-4)FT-IR
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