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Key Documents

226998

Sigma-Aldrich

Bromocyclobutane

96%

Synonym(s):

Cyclobutyl bromide

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About This Item

Empirical Formula (Hill Notation):
C4H7Br
CAS Number:
Molecular Weight:
135.00
Beilstein:
1900415
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

form

liquid

refractive index

n20/D 1.479 (lit.)

bp

108 °C (lit.)

density

1.434 g/mL at 25 °C (lit.)

SMILES string

BrC1CCC1

InChI

1S/C4H7Br/c5-4-2-1-3-4/h4H,1-3H2

InChI key

KXVUSQIDCZRUKF-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

71.6 °F - closed cup

Flash Point(C)

22 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yi Liu et al.
The journal of physical chemistry. A, 110(16), 5379-5385 (2006-04-21)
This study investigates the 234 nm photodissociation dynamics of cyclobutyl bromide using a two-dimensional photofragment velocity imaging technique. The spin-orbit ground- and excited-state Br(2P) atoms are state-selectively detected via [2+1] resonance enhanced multiphoton ionization (REMPI), whereas the cyclobutyl radicals are
Zhen Li et al.
Journal of medicinal chemistry, 48(20), 6169-6173 (2005-09-30)
A class of 3,5-diphenyl-1,2,4-oxadiazole based compounds have been identified as potent sphingosine-1-phosphate-1 (S1P1) receptor agonists with minimal affinity for the S1P2 and S1P3 receptor subtypes. Analogue 26 (S1P1 IC50 = 0.6 nM) has an excellent pharmacokinetics profile in the rat
Tao Guo et al.
Bioorganic & medicinal chemistry letters, 15(16), 3696-3700 (2005-06-28)
An encoded combinatorial library based on aryl and biaryl piperidine scaffolds was designed and synthesized. Screening of this library resulted in the discovery of high-nanomolar biaryl piperidine-based MCH1 receptor antagonists. Follow-up optimization using a parallel synthesis provided potent, single digit

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