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32796-33-1

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32796-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32796-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,9 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32796-33:
(7*3)+(6*2)+(5*7)+(4*9)+(3*6)+(2*3)+(1*3)=131
131 % 10 = 1
So 32796-33-1 is a valid CAS Registry Number.

32796-33-1SDS

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 phenyl(trimethylsilyl)phosphane

1.2 Other means of identification

Product number -
Other names Trimethylsilyl-phenylphosphin

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:32796-33-1 SDS

32796-33-1Relevant articles and documents

Tailoring Phospholes for Imprint of Fluorescent 3D Structures

Roesler, Fabian,Kaban, Burhan,Klintuch, Dieter,Ha, Uh-Myong,Bruhn, Clemens,Hillmer, Hartmut,Pietschnig, Rudolf

, p. 4820 - 4825 (2019)

PMMA based polymer blends have been infused with luminescent phospholes and have been structured via nanoimprint. While symmetrically substituted phospholes are prone to crystallization and phase separation, structural modification of the phosphole backbone in the α- and β-positions has been explored, which prevents these issues; a structural explanation for this is suggested. Best phase integrity has been obtained for β-silyl-substituted phospholes, which were implemented in thin films and beads. The emission wavelengths of the phospholes are shifted bathochromically in the polymer matrix as compared to the neat compounds featuring emission bands near 500 nm. This enables tracking of the fluorescent beads using standard fluorescence microscopy.

A nuclear magnetic resonance investigation of the bonding in fourth-group phenylphosphines

Harrison,Ulrich,Zuckerman

, p. 25 - 28 (2007/10/05)

The compounds (CH3)3MPHC6H5 where M = C, Si, and Sn have been synthesized, and J(31P-1H) values recorded. Infrared assignments in the region 4000-400 cm-1 are also presented. Controlled oxidation of the tin compound yields (CH3)3-SnOPHC6H5 as established by 31P couplings which also give information concerning the exchange of groups at phosphorus in mixtures of the two tin compounds. The one-bond 31P-1H couplings have been interpreted in terms of a pyramidal arrangement of bonds at phosphorus.

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