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1H-Borole, 2,5-dihydro-3,4-dimethyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112238-06-9

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112238-06-9 Usage

Chemical class

Belongs to the class of borole compounds.

Compound type

Heterocyclic compound containing boron, hydrogen, and carbon atoms.

Molecular weight

154.01 g/mol.

Physical state

Colorless liquid.

Odor

Pleasant, fruity.

Solubility

Insoluble in water, soluble in organic solvents.

Usage

Commonly used in organic synthesis and as a building block for pharmaceuticals and agrochemicals.

Potential applications

Shown potential in materials science, particularly in the development of new functional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 112238-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112238-06:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*8)+(2*0)+(1*6)=79
79 % 10 = 9
So 112238-06-9 is a valid CAS Registry Number.

112238-06-9SDS

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 3,4-dimethyl-1-phenyl-2,5-dihydroborole

1.2 Other means of identification

Product number -
Other names 1H-Borole,2,5-dihydro-3,4-dimethyl-1-phenyl

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:112238-06-9 SDS

112238-06-9Relevant academic research and scientific papers

Synthesis of C-substituted 2,5-Dihydro-1H-boroles (3-Borolenes)

Herberich, Gerhard E.,Marx, Hans-W.,Wagner, Trixie

, p. 2135 - 2140 (2007/10/02)

Magnesium-diene addition compounds derived from isoprene, 2,3-dimethylbutadiene, and 1,2-dimethylenecyclohexane are treated with boron halides BCl2(NR2) (R = Me, Et, iPr), PhBCl2, or MeBBr2 to give C-substituted 2,5-dihydro-1H-boroles (3-borolenes) 3-5.In a new in situ procedure 1,3-pentadiene reacts with Mg/BCl2(NR2) in THF to yield 2-methyl derivatives 2-MeC4H5BNR2 (2).The NMe3 adduct of 4,5,6,7-tetrahydro-2-methyl-2-boraindan 5e*NMe3 undergoes a topomerization with ΔG290(excit.) = 59 +/- 2 kJ/mol in a dissociative-associative process.The crystal structure of 3,4-dimethyl- 1-phenyl-3-borolene (4d) has been determined.The molecule displays a classical planar structure.There are no indications for specific intermolecular interactions. - Key Words: 1H-Boroles, 2,5-dihydro / 3-Borolenes / 2-Boraindan, 4,5,6,7-tetrahydro-

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