295183
Cyclopropane
≥99%
Synonym(s):
Trimethylene (6CI)
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About This Item
Empirical Formula (Hill Notation):
C3H6
CAS Number:
Molecular Weight:
42.08
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
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vapor density
1.45 (vs air)
Assay
≥99%
autoignition temp.
928 °F
expl. lim.
10.4 %
bp
−33 °C (lit.)
mp
−128 °C (lit.)
SMILES string
C1CC1
InChI
1S/C3H6/c1-2-3-1/h1-3H2
InChI key
LVZWSLJZHVFIQJ-UHFFFAOYSA-N
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Application
Cyclopropane has been used as the pseudo-π unsaturated hydrocarbon prototype to study the rotational spectrum of its complex formed with chlorine monofluoride and the similarity of this complex with isotopomers.
Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
Storage Class Code
2A - Gases
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Journal of medicinal chemistry, 55(18), 8028-8037 (2012-08-30)
Structure-based drug design can potentially accelerate the development of new therapeutics. In this study, a cocrystal structure of the acetylcholine binding protein (AChBP) from Capitella teleta (Ct) in complex with a cyclopropane-containing selective α4β2-nicotinic acetylcholine receptor (nAChR) partial agonist (compound
Pedro S Coelho et al.
Science (New York, N.Y.), 339(6117), 307-310 (2012-12-22)
Transition metal-catalyzed transfers of carbenes, nitrenes, and oxenes are powerful methods for functionalizing C=C and C-H bonds. Nature has evolved a diverse toolbox for oxene transfers, as exemplified by the myriad monooxygenation reactions catalyzed by cytochrome P450 enzymes. The isoelectronic
A pseudo-? analogue of a Mulliken b?. a? type complex: The rotational spectrum of cyclopropane?chlorine monofluoride.
Holloway JH & Legon AC.
J. Chem. Soc., Faraday Trans., 93(3), 373-378 (1997)
Yoshihiro Oonishi et al.
Angewandte Chemie (International ed. in English), 51(29), 7305-7308 (2012-06-29)
Giving direction: An C sp 3-H bond activation directed by a rhodacycle intermediate has been found to occur in a Rh(I)-catalyzed reaction between an allene moiety having a tert-butyl substituent, and tethered alkynes. Cyclic compounds containing a cyclopropane ring were obtained in
Shuhei Kawamura et al.
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The natural product belactosin A (1) with a trans-cyclopropane structure is a useful prototype compound for developing potent proteasome (core particle, CP) inhibitors. To date, 1 and its analogues are the only CP ligands that bind to both the nonprimed
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