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3,3-Dimethylcyclopropene is a cyclic hydrocarbon compound with the molecular formula C5H8. It features a three-carbon ring structure with two methyl groups (CH3) attached to the same carbon atom within the ring. This organic compound is known for its unique chemical properties, such as high reactivity and strain in the molecule due to the presence of the cyclopropane ring. 3,3-Dimethylcyclopropene is an important intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity arises from the ring strain, which makes it a valuable building block for constructing more complex molecules.

3907-06-0

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3907-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3907-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3907-06:
(6*3)+(5*9)+(4*0)+(3*7)+(2*0)+(1*6)=90
90 % 10 = 0
So 3907-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H8/c1-5(2)3-4-5/h3-4H,1-2H3

3907-06-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethylcyclopropene

1.2 Other means of identification

Product number -
Other names Cyclopropene,3,3-dimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3907-06-0 SDS

3907-06-0Relevant articles and documents

Tandem Hydroalumination/Cu-Catalyzed Asymmetric Vinyl Metalation as a New Access to Enantioenriched Vinylcyclopropane Derivatives

Müller, Daniel S.,Werner, Veronika,Akyol, Sema,Schmalz, Hans-Günther,Marek, Ilan

supporting information, p. 3970 - 3973 (2017/08/14)

Herein, we report the first enantio- and diastereoselective addition of stereodefined vinyl organometallic reagents to cyclopropenes. The operationally simple tandem hydroalumination and copper-catalyzed vinylmetalation allows for the unique access of a diverse set of enantioenriched vinylcyclopropane derivatives.

Stereocontrolled approaches to 2-(2-aminoalkyl)-1-hydroxycyclopropanes

Baird, Mark S,Huber, Florian A.M,Clegg, William

, p. 9849 - 9858 (2007/10/03)

(1S,2S)-2[(S)-Amino(4-methoxyphenyl)methyl]cyclopropan-1-ol together with a range of racemic 2-(2-aminoalkyl)-1-hydroxycyclopropanes were prepared by a stepwise procedure involving a 1,3-dipolar cycloaddition of a nitrile oxide to a cyclopropene followed

New complexes of platinum(0) with cyclopropenes

Hughes, David L.,Leigh, G. Jeffery,McMahon, C. Niamh

, p. 1301 - 1307 (2007/10/03)

New cyciopropene complexes of platinum have been synthesised with a variety of bulky substituents on all positions of the cyciopropene ring. Two of these novel complexes, [Pt(3,3-Ph3C3H2)(PPh3)2] and [Pt(1,2-Ph2C3H2)(PPh3)2J, have been structurally characterised by X-ray analysis. Both contain a cyciopropene ring which has remained intact upon complexation. The bond lengths within the complexes are remarkably independent of the substituents. The structural characteristics and the 31P NMR spectra of these complexes are discussed in detail.

SELECTIVITY IN THE REACTIONS OF 3,3-DISUBSTITUTED CYCLOPROPENES WITH NITRILE OXIDES

Bolesov, I. G.,Ignatchenko, A. V.,Bovin, N. V.,Prudchenko, I. A.,Surmina, L. S.,et al.

, p. 87 - 100 (2007/10/02)

The reactions of 3-R-3-R'-disubstituted cyclopropenes with nitrile oxides lead to the formation of 4,6,6-trisubstituted 2-oxa-3-azabicyclohex-3-enes, which can be isolated with high yields.Substituents at C3 of the cyclopropane ring (phe

Reaktion von 1,2,4,5-Tetrazin-3,6-dicarbonsaeure-dimethylester mit 3,3-Dimethylcyclopropen: Unerwartete Bildung eines -Addukts

Huber, Franz-Xaver,Sauer, Juergen,McDonald, Walter S.,Noeth, Heinrich

, p. 444 - 451 (2007/10/02)

Reaction of tetrazine 1 with 3,3-dimethylcyclopropene (2) at lower temperature leads to the expected products 3 and 4; in addition a -adduct 7 is isolated at higher temperature (>80 deg C).Its structure was ascertained by spectroscopic data and X-ray structure analysis.

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