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359890

Sigma-Aldrich

Dimethyl bromomalonate

technical grade, 90%

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About This Item

Linear Formula:
BrCH(COOCH3)2
CAS Number:
868-26-8
Molecular Weight:
211.01
Beilstein:
971135
EC Number:
212-775-4
MDL number:
MFCD00025865
UNSPSC Code:
12352100
PubChem Substance ID:
24862117
NACRES:
NA.22

grade

technical grade

Quality Level

100

Assay

90%

form

liquid

refractive index

n20/D 1.460 (lit.)

bp

105-108 °C/11 mmHg (lit.)

density

1.601 g/mL at 25 °C (lit.)

functional group

bromo
ester

SMILES string

COC(=O)C(Br)C(=O)OC

InChI

1S/C5H7BrO4/c1-9-4(7)3(6)5(8)10-2/h3H,1-2H3

InChI key

NEMOJKROKMMQBQ-UHFFFAOYSA-N

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General description

Dimethyl bromomalonate undergoes manganese(III)-promoted free-radical chain addition reaction with olefins, to yield dimethyl 2-bromoalkylmalonates. Organocatalyzed Michael addition of dimethyl bromomalonate to nitrostyrenes to yield synthetically useful nitrocyclopropanes has been reported. Dimethyl bromomalonate reacts readily with arylnitroso compounds to yield the corresponding N-aryl-C,C-dimethoxycarbonylnitrones.

Application

Dimethyl bromomalonate may be used in the enantioselective synthesis of nitrocyclopropanes.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

359890-25ML:
359890-5ML:
359890-BULK:
359890-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBZ1254V
MKBR5978V
MKBC9135V
MKBC9135
07008AH

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Synthesis and 1, 3-dipolar cycloaddition reactions of N-aryl-C, C-dimethoxycarbonylnitrones.
Tomioka Y, et al.
Journal of Heterocyclic Chemistry, 40(1), 121-128 (2003)
Yi-Ning Xuan et al.
Organic letters, 11(7), 1583-1586 (2009-03-06)
Highly enantioselective synthesis of nitrocyclopropanes was achieved via the organocatalytic conjugate addition of dimethyl bromomalonate to nitroalkenes and the consequent intramolecular cyclopropanation. 6'-Demethyl quinine was found to be the efficient catalyst. Excellent enantioselectivities, diastereoselectivities, and good yields were obtained for
Stereoselective synthesis of functionalised cyclopropanes from nitroalkenes via an organocatalysed Michael-initiated ring-closure approach.
Russo A and Lattanzi A.
Tetrahedron Asymmetry, 21(9), 1155-1157 (2010)
Manganese (III)-promoted free-radical addition of dimethyl bromomalonate to olefins using an electrochemical regeneration procedure.
Nedelec JY and Nohair K.
Synlett, 09, 659-660 (1991)

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