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1H-Phosphole, 3-methyl-1-[2,4,6-tris(1-methylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191548-31-9

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191548-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191548-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,4 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191548-31:
(8*1)+(7*9)+(6*1)+(5*5)+(4*4)+(3*8)+(2*3)+(1*1)=149
149 % 10 = 9
So 191548-31-9 is a valid CAS Registry Number.

191548-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-[2,4,6-tri(propan-2-yl)cyclohexyl]phospholane

1.2 Other means of identification

Product number -
Other names 1H-Phosphole,3-methyl-1-[2,4,6-tris(1-methylethyl)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:191548-31-9 SDS

191548-31-9Upstream product

191548-31-9Relevant academic research and scientific papers

Phospholes with reduced pyramidal character from steric crowding III NMR and X-ray diffraction studies on 1-( 2,4,6-tri-isopropylphenyl)-3-methylphosphole

Keglevich, Gyoergy,Quin, Louis D.,Boecskei, Zsolt,Keserue, Gyoergy M.,Kalgutkar, Rajdeep,Lahti, Paul M.

, p. 109 - 116 (1997)

The 2,4,6-tri-isopropylphenyl substituent was placed on the phosphorus of a phosphole to reduce the pyramidal character. That this was accomplished was revealed by single crystal X-ray diffraction analysis; with respect to the plane of C2-P-C5 in the phosphole ring, the ipso carbon of the benzene ring was deflected by only 58.0°, whereas the deflection is 66.9° in the uncrowded 1-benzylphosphole. This proves that the concept of reducing the pyramidal character (with the goal of increasing the electron delocalization) through steric crowding can be realized. In the crystal the two rings are in orthogonal planes, but this relation is not retained in solution; NMR studies show that the two edges of the benzene ring, as well as the 2,6-isopropyl groups, are identical.

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