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38557-29-8

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38557-29-8 Usage

General Description

Iodocyclobutane is a type of organic compound within the field of chemistry. Its chemical formula is C4H7I, indicating it is composed of carbon, hydrogen, and iodine elements. This molecule falls into the category of halocycloalkanes, specifically an iodocycloalkane, as it is a cycloalkane with an iodine atom attached. The presence of the iodine atom makes it susceptible to various reactions, particularly substitution reactions. Little information is publicly available on the specific properties or applications of iodocyclobutane, but like other iodocycloalkanes, it could potentially be used in various chemical synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 38557-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,5 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38557-29:
(7*3)+(6*8)+(5*5)+(4*5)+(3*7)+(2*2)+(1*9)=148
148 % 10 = 8
So 38557-29-8 is a valid CAS Registry Number.

38557-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name iodocyclobutane

1.2 Other means of identification

Product number -
Other names cyclobutyl iodide

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:38557-29-8 SDS

38557-29-8Relevant articles and documents

Vibrational Spectra and Conformations of (Iodomethyl)cyclopropane and Epiiodohydrin

Wurrey, C. J.,Yeh, Y. Y.,Krishnamoorthi, R.,Berry, R. J.,DeWitt, J. E.,Kalasinsky, V. F.

, p. 4059 - 4063 (1984)

The infrared (4000-400 cm-1) spectra of (iodomethyl)cyclopropane and epiiodohydrin in all three physical states have been recorded.The Raman (3500-50 cm-1) spectra of these two molecules in condensed phases have also been obtained.For (iodomethyl)cyclopropane no multiple Q branches were observed in the gase-phase infrared spectrum nor were any liquid-phase peaks observed to vanish upon crystallization.On the basis of these data and on the liquid-phase Raman depolarization ratios (which suggest that all observed Raman lines are polarized) it has been concluded that (iodomethyl)cyclopropane exists solely in the (nonsymmetric) gauche conformation in all states of matter.On the other hand, epiiodohydrin exhibits several gas-phase infrared band contours with "extra" Q branches and ten liquid-phase Raman conformer doublets, wherein one member of each doublet disappears when the annealed solid phase is obtained.These data have been interpreted in terms of a gauche-1 (70percent)/gauche-2 (30percent) conformational equilibrium for liquid epiiodohydrin at room temperature, with only the gauche-1 conformer remaining in the crystalline sample.From a variable-temperature (-74 to 25 deg C) study of the base-line-resolved liquid-phase Raman doublet at 940/914 cm-1, an enthalpy difference between conformers of 0.50 +/- 0.05 kcal/mol has been determined, with the gauche-1 conformer the more stable.No evidence for a cis conformation of either molecule was found, apparently as a result of strong steric interactions between the iodine atom and β-ring hydrogen atoms.For these molecules, vibrational assignments, which are in excellent agreement with the vibrational assignments of other (halomethyl)cyclopropanes and epihalohydrins, have also been proposed.

ELECTROPHILIC ADDITION TO BICYCLOBUTANE>

Abramova, N. M.,Zotova, S. V.,Nesmeyanova, O. A.

, p. 961 - 964 (2007/10/02)

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