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1-Bromo-2-ethylbutane_Molecular_structure_CAS_3814-34-4)
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1-Bromo-2-ethylbutane

Catalog No. 252263 Name Sigma Aldrich
CAS Number 3814-34-4 Website http://www.sigmaaldrich.com
M. F. C6H13Br Telephone 1-800-521-8956
M. W. 165.07142 Fax
Purity 97% Email
Storage Chembase ID: 90184

SYNONYMS

Title
1-溴-2-乙基丁烷
IUPAC name
3-(bromomethyl)pentane
IUPAC Traditional name
3-(bromomethyl)pentane
Synonyms
3-(溴甲基)戊烷
3-(Bromomethyl)pentane

DATABASE IDS

MDL Number MFCD00000219
PubChem SID 24855195
EC Number 223-302-6
CAS Number 3814-34-4

PROPERTIES

Linear Formula (C2H5)2CHCH2Br
Purity 97%
Boiling Point 143-144 °C(lit.)
Density 1.179 g/mL at 25 °C(lit.)
Flash Point 36 °C
Flash Point 96.8 °F
Refractive Index n20/D 1.4498(lit.)
GHS Pictograms GHS02
GHS Signal Word Warning
GHS Hazard statements H226
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
RID/ADR UN 1993 3/PG 3
Risk Statements 10
Safety Statements 16-29-33
Hazard Class 3
UN Number 1993
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5, 25 mL in glass bottle
Application
Reactant involved in the synthesis of biologically active molecules including:
• Nantenine analogs with aporphinoid 5-HT2A and α-1A antagonistic activity1
• Aporphines with cytotoxicity toward human colon cancer cell lines2
• Dimeric amide foldamers acting as alpha-helix mimetics3
• Endocrine-disrupting nanylphenol isomers synthesized via demethylation4
• Phosphonic acid-containing benzimidazoles for use as fructose-1,6-biphosphatase inhibitors5
• 5-Bromo-1H-indole-3-acetohydroxamic acid for use as peptide deformylase inhibitors6Reactant involved in studies of the effect of oxygenated side chains in Ephedra compounds7
Description (简体中文)
包装
5, 25 mL in glass bottle
Application
Reactant involved in the synthesis of biologically active molecules including:
• Nantenine analogs with aporphinoid 5-HT2A and α-1A antagonistic activity1
• Aporphines with cytotoxicity toward human colon cancer cell lines2
• Dimeric amide foldamers acting as alpha-helix mimetics3
• Endocrine-disrupting nanylphenol isomers synthesized via demethylation4
• Phosphonic acid-containing benzimidazoles for use as fructose-1,6-biphosphatase inhibitors5
• 5-Bromo-1H-indole-3-acetohydroxamic acid for use as peptide deformylase inhibitors6Reactant involved in studies of the effect of oxygenated side chains in Ephedra compounds7

REFERENCES