Skip to Content
Merck
CN

274372

3,3-Dimethylallyl bromide

95%, contains silver wool as stabilizer

Synonym(s):

1-Bromo-3-methyl-2-butene, Prenyl bromide

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
(CH3)2C=CHCH2Br
CAS Number:
Molecular Weight:
149.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-799-5
Beilstein/REAXYS Number:
1420778
MDL number:
Assay:
95%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

LOYZVRIHVZEDMW-UHFFFAOYSA-N

InChI

1S/C5H9Br/c1-5(2)3-4-6/h3H,4H2,1-2H3

SMILES string

C\C(C)=C\CBr

assay

95%

contains

silver wool as stabilizer

Quality Level

bp

82-83 °C/150 mmHg (lit.)

density

1.29 g/mL at 20 °C (lit.)

functional group

alkyl halide, bromo

storage temp.

2-8°C

Looking for similar products? Visit Product Comparison Guide

Application

3,3-Dimethylallyl bromide was used in the synthesis of 1- and 2-allylic-3-methylindoles. It was also used in the synthesis of products and base-modified pyrimidine nucleosides.

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

104.0 °F - closed cup

flash_point_c

40 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Electrophilic substitution in indoles?I: Model experiments related to the synthesis of echinulin.
Tetrahedron, 21(5), 989-1000 (1965)
Tetrahedron, 49, 2533-2533 (1993)
Journal of the Chemical Society. Perkin Transactions 1, 1153-1153 (1993)
Kamal Rullah et al.
Bioorganic & medicinal chemistry letters, 24(16), 3826-3834 (2014-07-17)
The discovery of potent inhibitors of prostaglandin E2 (PGE2) synthesis in recent years has been proven to be an important game changer in pharmaceutical industry. It is known that excessive production of PGE2 triggers a vast array of biological signals

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