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335819

Sigma-Aldrich

Ethyl 3-bromobenzoate

98%

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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
Pricing and availability is not currently available.

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

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This Item
0997-PA0859-PA0070-PA
3`SLN-C3-PAA

0036-PA

3`SLN-C3-PAA

6`SLN-C3-PAA

0997-PA

6`SLN-C3-PAA

(3`-suLN)3`LN-C3-PAA

0859-PA

(3`-suLN)3`LN-C3-PAA

Galα3`LN-C3-PAA

0070-PA

Galα3`LN-C3-PAA

probe type

trisaccharide

probe type

trisaccharide

probe type

tetrasaccharide

probe type

trisaccharide

carrier

PAA carrier

carrier

PAA carrier

carrier

PAA carrier

carrier

PAA carrier

probe presentation

polymeric

probe presentation

polymeric

probe presentation

polymeric

probe presentation

polymeric

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

product line

PA-Series

product line

PA-Series

product line

PA-Series

product line

PA-Series

assay

95% (H-NMR)

assay

95% (H-NMR)

assay

95% (H-NMR)

assay

95% (H-NMR)

Application

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

  • Specification Sheet

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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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