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22409-26-3

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22409-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22409-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,0 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22409-26:
(7*2)+(6*2)+(5*4)+(4*0)+(3*9)+(2*2)+(1*6)=83
83 % 10 = 3
So 22409-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H25NSi/c1-17(2,15-9-5-3-6-10-15)14-13-16-11-7-4-8-12-16/h3,5-6,9-10H,4,7-8,11-14H2,1-2H3

22409-26-3SDS

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 dimethyl-phenyl-(2-piperidin-1-ylethyl)silane

1.2 Other means of identification

Product number -
Other names Sdk-50

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:22409-26-3 SDS

22409-26-3Downstream Products

22409-26-3Relevant articles and documents

NITROGEN-CONTAINING ORGANOSILICON COMPOUNDS. 150. SYNTHESIS AND CHROMATOGRAPHIC AND 1H, 13C, 15N, AND 29Si NMR SPECTROSCOPIC INVESTIGATION OF SUBSTITUTED (PIPERIDINOALKYL)SILANES

Lukevits, E.,Sleiksha, I.,Liepin'sh, E.,Shats-ts, V. D.,Zitsmane, I.,Purvinya, A.

, p. 1319 - 1327 (1991)

Substituted (piperidinoalkyl)silanes were synthesized and investigated by means of multinuclear NMR spectroscopy and GLC.The data obtained indicate an additional N-Si interaction in α-aminomethylsilanes that depends substantially on the properties of the substituents attached to the silicon atom.The effect of the R1R2R3Si substituent on the capacity of the nitrogen atom for intermolecular interactions is not restricted to steric effects but also has electronic character.

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