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335800

Sigma-Aldrich

Ethyl 2-bromobenzoate

98%

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About This Item

Linear Formula:
BrC6H4CO2C2H5
CAS Number:
6091-64-1
Molecular Weight:
229.07
EC Number:
228-034-3
MDL number:
MFCD00015443
UNSPSC Code:
12352100
PubChem Substance ID:
24860348

Assay

98%

form

liquid

refractive index

n20/D 1.544 (lit.)

bp

117 °C/17 mmHg (lit.)

density

1.443 g/mL at 25 °C (lit.)

functional group

bromo
ester

SMILES string

CCOC(=O)c1ccccc1Br

InChI

1S/C9H9BrO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6H,2H2,1H3

InChI key

BIHHBTVQFPVSTE-UHFFFAOYSA-N

General description

Ethyl 2-bromobenzoate is an halobenzoic acid ethyl ester. Silylation and hydrolysis of ethyl 2-bromobenzoate has been reported.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

335800-VAR:
335800-100G:
335800-BULK:
335800-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS5620V
BCBG8385V
1402183V
1448825V
1448825

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Gernot A Eller
Molecules (Basel, Switzerland), 11(11), 915-928 (2007-11-17)
This work deals with the use of organic systematic nomenclature in scientific literature, its quality, and computerized methods for its improvement. Criteria for classification of systematic names in terms of quality/correctness are discussed and applied to a sample set of
Scott E Denmark et al.
Organic letters, 5(19), 3483-3486 (2003-09-12)
[reaction: see text] A mild and general palladium-catalyzed insertion of 1,2-diethoxy-1,1,2,2-tetramethyldisilane into a variety of aryl bromides affords the aryldimethylsilyl ethers in high yields. Hydrolysis of the ethers under pH-optimized conditions results in the exclusive formation of the desired aryldimethylsilanols.

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