Skip to Content
Merck
All Photos(1)

Documents

364878

Sigma-Aldrich

1-Bromocarbonyl-1-methylethyl acetate

≥95.0%

Synonym(s):

α-Acetoxyisobutyryl bromide, 2-Acetoxy-2-methylpropionyl bromide

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3COOC(CH3)2COBr
CAS Number:
Molecular Weight:
209.04
Beilstein:
2432585
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥95.0%

refractive index

n20/D 1.457 (lit.)

bp

75-77 °C/12 mmHg (lit.)

density

1.431 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(=O)OC(C)(C)C(Br)=O

InChI

1S/C6H9BrO3/c1-4(8)10-6(2,3)5(7)9/h1-3H3

InChI key

OOKAXSHFTDPZHP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

1-Bromocarbonyl-1-methylethyl acetate (α-Acetoxyisobutyryl bromide) participates in the conversion of adenosine to trans-3′(2′)-bromo-2′(3′)-acetates, via glycosyl cleavage.

Application

1-Bromocarbonyl-1-methylethyl acetate (α-Acetoxyisobutyryl bromide) may be used:
  • in the chemoenzymatic synthesis of (1R,2S)-1,2-epoxy-1,2-dihydroacridine (acridine 1,2-oxide)
  • in the synthesis of protected 3′-deoxyadenosine and 3′-deoxyguanosine
  • as reagent for deoxygenation of vicinal diols, as well as in the preparation of 2′,3′-dideoxycytidine and other dideoxy and deoxynucleosides from the corresponding ribo series.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Aldrichimica Acta, 23, 83-83 (1990)
Biphenyl dioxygenase-catalysed cis-dihydroxylation of tricyclic azaarenes: chemoenzymatic synthesis of arene oxide metabolites and furoquinoline alkaloids.
Boyd DR, et al.
Royal Society of Chemistry Advances, 3(27), 10944-10955 (2013)
A mild conversion of vicinal diols to alkenes. Efficient transformation of ribonucleosides into 2'-ene and 2t', 3'-dideoxynucleosides.
Robins MJ, et al.
Tetrahedron Letters, 25(4), 367-370 (1984)
Efficient synthesis of protected 3'-deoxyadenosine and 3'-deoxyguanosine from adenosine and guanosine.
Cui Z, et al.
Tetrahedron Letters, 42(4), 561-563 (2001)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service