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335819

Sigma-Aldrich

Ethyl 3-bromobenzoate

98%

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25 G
¥31,600

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25 G
¥31,600

About This Item

Linear Formula:
BrC6H4CO2C2H5
CAS Number:
24398-88-7
Molecular Weight:
229.07
EC Number:
246-223-9
MDL number:
MFCD00013529
UNSPSC Code:
12352100
PubChem Substance ID:
24860350
NACRES:
NA.22

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Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.541 (lit.)

bp

130-131 °C/12 mmHg (lit.)

density

1.431 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)c1cccc(Br)c1

InChI

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

InChI key

QAUASTLEZAPQTB-UHFFFAOYSA-N

Related Categories

Application

Ethyl 3-bromobenzoate was used in the preparation of ethyl 3-ethynylbenzoate.[1]

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.

JAN Code

335819-100G:
335819-5G:
335819-BULK:
335819-25G:
335819-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBR7094V
MKBL6144V
MKBH4456V
04911HJ
08714TH

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T Iijima et al.
Chemical & pharmaceutical bulletin, 47(3), 398-404 (1999-04-23)
Synthesis and biological evaluation of the first dicarba-closo-dodecaborane (carborane) derivatives of retinoids are described. Their retinoidal activity were examined in terms of the differentiation-inducing ability toward human promyelocytic leukemia HL-60 cells. High retinoidal activity (agonist or antagonist for retinoic acid

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