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498963

Sigma-Aldrich

Isobutylzinc bromide solution

0.5 M in THF

Synonym(s):

(2-Methylpropyl)zinc bromide, Bromo(2-methylpropyl)zinc

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1 G
₹12,991.00

₹12,991.00


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1 G
₹12,991.00

About This Item

Linear Formula:
(CH3)2CHCH2ZnBr
CAS Number:
Molecular Weight:
202.41
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

₹12,991.00


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Quality Level

concentration

0.5 M in THF

density

0.943 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

CC(C)C[Zn]Br

InChI

1S/C4H9.BrH.Zn/c1-4(2)3;;/h4H,1H2,2-3H3;1H;/q;;+1/p-1

InChI key

WYBHVVXVUCUWSE-UHFFFAOYSA-M

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This Item
202112004220265
material

W,W,F separators

material

W,GFF,F separators

material

W,W,W separators

material

GFF,F,F separators, silica gel

composition

Bed A, 400 mg , Bed B, 200 mg

composition

Bed A, 400 mg , Bed B, 200 mg

composition

Bed A, 100 mg , Bed B, 50 mg

composition

Bed A, 400 mg , Bed B, 200 mg

agency

ASTM® D3686, OSHA ID-186SG, NIOSH 1001,1006,1009,1017,1018,1024,1606,1615,2516,2519

agency

NIOSH 6013

agency

OSHA 56

agency

NIOSH 2011,7903, OSHA ID-165SG,ID-174SG

technique(s)

active air sampling: suitable

technique(s)

active air sampling: suitable

technique(s)

active air sampling: suitable

technique(s)

active air sampling: suitable

product line

ORBO

product line

ORBO

product line

ORBO

product line

ORBO

packaging

pkg of 50 ea

packaging

pkg of 25 ea

packaging

pkg of 50 ea

packaging

pkg of 50 ea

Application

Isobutylzinc bromide is an organozinc compound, which can be used as a reagent in the palladium-catalyzed Negishi cross-coupling reaction to construct a carbon-carbon bond by reacting with aryl or heteroaryl halides [1][2]. It is also used to prepare regioselective unsaturated ketones by reacting with tert-butyl isocyanide via an allylic carbonylative coupling reaction in the presence of a nickel catalyst.[2]

Legal Information

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3 - Water-react 2

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 3

Flash Point(F)

1.4 °F - closed cup

Flash Point(C)

-17.0 °C - closed cup


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    T C Tallant et al.
    Journal of bacteriology, 179(22), 6902-6911 (1997-11-26)
    During growth on acetate, Methanosarcina barkeri expresses catabolic enzymes for other methanogenic substrates such as monomethylamine. The range of substrates used by cells grown on acetate was further explored, and it was found that cells grown on acetate also converted
    Determination of enantiomeric purity of 3-mercapto-2-methylpropionic acid.
    D Wang-Iverson et al.
    Journal of chromatography, 408, 365-371 (1987-11-06)
    H G Brittain et al.
    Pharmaceutical research, 7(10), 1082-1085 (1990-10-01)
    The ultraviolet and circular dichroism spectra of authentic captopril have been obtained, since the reported literature data are inconsistent with those obtained on highly purified material. The UV absorption spectrum consists of a single band maximum at 200 nm, while
    M R Smith et al.
    Bioorganic & medicinal chemistry, 2(7), 589-593 (1994-07-01)
    A bacterium (strain photoB) photoassimilated 3-mercapto-2-methylpropionate as sole source of sulphur with methacrylate accumulating in the medium. This was thought to be the product of a sulphur-lyase type enzyme attacking the 3-mercapto-2-methylpropionate. Detailed examination of the biochemistry of the utilization
    Erinn C Howard et al.
    Science (New York, N.Y.), 314(5799), 649-652 (2006-10-28)
    Flux of dimethylsulfide (DMS) from ocean surface waters is the predominant natural source of sulfur to the atmosphere and influences climate by aerosol formation. Marine bacterioplankton regulate sulfur flux by converting the precursor dimethylsulfoniopropionate (DMSP) either to DMS or to

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