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704040

Sigma-Aldrich

3-(Bromoacetyl)pyridine hydrobromide

95%

Synonym(s):

2-Bromo-1-(3-pyridyl)ethanone hydrobromide

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About This Item

Linear Formula:
C7H6BrNO · HBr
CAS Number:
17694-68-7
Molecular Weight:
280.94
EC Number:
241-692-6
MDL number:
MFCD00052182
UNSPSC Code:
12352100
PubChem Substance ID:
329762088

Assay

95%

form

solid

mp

192-197 °C

functional group

bromo
ketone

SMILES string

Br.BrCC(=O)c1cccnc1

InChI

1S/C7H6BrNO.BrH/c8-4-7(10)6-2-1-3-9-5-6;/h1-3,5H,4H2;1H

InChI key

WDTSYONULAZKIE-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBL2925V
SHBC4284V
MKBH0469V
MKBG2454V
MKBF6230V

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W Ulmer et al.
European journal of biochemistry, 136(1), 183-194 (1983-10-17)
Bromoacetylpyridine acts as an active-site-directed inhibitor on glucose dehydrogenase from Bacillus megaterium. The inactivation is irreversible with a Ki of 7.7 mM. The coenzyme NAD but not the substrate glucose protects the enzyme from the inactivation. It is proposed that

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