CAS 22037-28-1|3-bromofuran|3-bromofuran|3-Bromofuran|3-Bromofuran, stabilized with Copper (0.1%), Furan (0.5%) and Sodium Hydrogen Carbonate (0.4%)|3-Furyl bromide|<i>beta</i>-Bromofuran|3-溴呋喃|3...

InChI=1S/C4H3BrO/c5-4-1-2-6-3-4/h1-3H

LXWLEQZDXOQZGW-UHFFFAOYSA-N

H Acceptors

H Donor

LogD (pH = 5.5)

1.882244

LogD (pH = 7.4)

1.882244

Log P

1.882244

Molar Refractivity

26.1942

Polarizability

10.210459

Polar Surface Area

13.14

Rotatable Bonds

Lipinski's Rule of Five

true

IUPAC Traditional name

3-Bromofuran3-Bromofuran, stabilized with Copper (0.1%), Furan (0.5%) and Sodium Hydrogen Carbonate (0.4%)3-Furyl bromidebeta-Bromofuran3-溴呋喃3-Bromofuranβ-Bromofuran

Highly Flammable/Irritant/Light Sensitive/Store at -20°C

Danger

Flammable (F)

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176524

Packaging
2.5, 10 g in glass bottle

B684510

3-Bromofuran is heterocyclic building block used in organic synthesis. 3-Bromofuran is one of the volatile metabolites discussed in studies for detecting and discriminating diseases of onion.

• Prithiviraj, B. et al.: Eur. J. Plant Pathol., 110, 371 (2004)

• Precursor of 3-lithiofuran by treatment with n-BuLi at low temperatures. Isomerization to 2-lithiofuran tends to occur above -40^o: Tetrahedron, 46, 1199 (1990). With LDA at -78^o, selective 2-lithiation can be achieved to give 3-bromo-2-lithiofuran, which has been used in synthesis of phenethylthiazolylthiourea (PETT) analogues as potential HIV-1 reverse transcriptase inhibitors: J. Med. Chem., 39, 4261 (1996).

Names and Identifiers

IUPAC Traditional name

3-bromofuran

IUPAC name

3-bromofuran

Synonyms

3-Bromofuran3-Bromofuran, stabilized with Copper (0.1%), Furan (0.5%) and Sodium Hydrogen Carbonate (0.4%)3-Furyl bromidebeta-Bromofuran3-溴呋喃3-Bromofuranβ-Bromofuran

Registration numbers

CAS Number

Wikipedia Title

Chemspider ID

PubChem CID

Beilstein Number

MDL Number

EC Number

PubChem SID

Molecule Details

176524

Packaging
2.5, 10 g in glass bottle

TRC

B684510

3-Bromofuran is heterocyclic building block used in organic synthesis. 3-Bromofuran is one of the volatile metabolites discussed in studies for detecting and discriminating diseases of onion.

References

PubChem Literature

From Data Sources

• Prithiviraj, B. et al.: Eur. J. Plant Pathol., 110, 371 (2004)

Bioactivity

PubChem BioAssay

Irritant (Xi)

GHS Pictograms

Flammable gases, category 1

Flammable aerosols, categories 1,2

Flammable liquids, categories 1,2,3

Self-reactive substances and mixtures, Types B,C,D,E,F

Pyrophoric liquids, category 1

Pyrophoric solids, category 1

Self-heating substances and mixtures

Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3

Organic peroxides, Types B,C,D,E,F

Acute toxicity (oral, dermal, inhalation), category 4

Skin irritation, category 2

Eye irritation, category 2

Skin sensitisation, category 1

Specific Target Organ Toxicity – Single exposure, category 3

GHS Hazard statements

H225

H225-H315-H319-H335

Risk Statements

11-36/37/38

RID/ADR

UN 1993 3/PG 2

Storage Temperature

-20°C

Packing Group

German water hazard class

MSDS Link

Download link

GHS Precautionary statements

P210

P210-P241-P303+P361+P353-P305+P351+P338-P405-P501A

Personal Protective Equipment

Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter

Hazard Class

UN Number

1993

UN1993

Safety Statements

16-23-24/25

9-16-26-37-60

TSCA Listed

否

Hydrophobicity(logP)

European Hazard Symbols

Empirical Formula (Hill Notation)

Certificate of Analysis

Molecule

ID:80499