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1501-58-2

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1501-58-2 Usage

Type of compound

Cyclic alkene

Ring structure

Four-membered ring

Substituents

Two methyl groups attached to the first and second carbon atoms

Physical state

Liquid

Reactivity

Highly reactive

Flammability

Flammable

Natural occurrence

Not commonly found in nature

Synthesis

Can be synthesized in a laboratory setting

Applications

Organic chemistry research, building block for synthesis of other organic compounds

Industries

Pharmaceutical and agrochemical industries

Molecular structure significance

Unique molecular structure, subject of interest for further study in chemical synthesis and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 1501-58-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1501-58:
(6*1)+(5*5)+(4*0)+(3*1)+(2*5)+(1*8)=52
52 % 10 = 2
So 1501-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10/c1-5-3-4-6(5)2/h3-4H2,1-2H3

1501-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethylcyclobutene

1.2 Other means of identification

Product number -
Other names Cyclobutene,1,2-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:1501-58-2 SDS

1501-58-2Relevant articles and documents

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Cornelisse,J. et al.

, p. 6197 - 6203 (1973)

-

Murov et al.

, p. 4329,4330, 4331 (1973)

The Geometries of the s-Cis Conformers of Some Acyclic 1,3-Dienes: Planar or Twisted?

Squillacote, Michael E.,Semple, Thomas C.,Mui, Philip W.

, p. 6842 - 6846 (1985)

We have established a method to determine the geometry of the minor forms of acyclic 1,3-dienes.A high vacuum cryogenic trapping technique was used to obtain spectral data of these metastable conformers from mixtures equilibrated at 1100 K.This has enabled us to characterize the minor form of 2,3-dimethyl-1,3-butadiene (DMB) by IR and UV spectroscopy.Barriers to rotation of the metastable forms of isoprene and DMB to their stable s-trans forms have also been obtained.The UV spectra of acyclic 1,3-dienes are found to be determinant of structure and, on this basis, weassign a planar s-cis molecular framework to 1,3-butadiene and isoprene, and a gauche s-cis geometry to DMB.

Selective Isomerization of Butadiene-Cyclobutene Systems via Infrared Multiphoton Excitation

Buechele, James L.,Weitz, Eric,Lewis, Frederick D.

, p. 3588 - 3589 (1981)

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