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73992-96-8

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73992-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73992-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73992-96:
(7*7)+(6*3)+(5*9)+(4*9)+(3*2)+(2*9)+(1*6)=178
178 % 10 = 8
So 73992-96-8 is a valid CAS Registry Number.

73992-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl<(4-methyl-1-piperazinyl)methyl>silane

1.2 Other means of identification

Product number -
Other names 1-Methyl-4-trimethylsilanylmethyl-piperazine

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:73992-96-8 SDS

73992-96-8Relevant articles and documents

Selective 1,2-Aryl-Aminoalkylation of Alkenes Enabled by Metallaphotoredox Catalysis

Chen, Zimin,Hu, Yuanyuan,Li, Weirong,Liao, Zixuan,Xi, Xiaoxiang,Yuan, Weiming,Zheng, Songlin

supporting information, p. 17910 - 17916 (2020/08/21)

A highly chemo- and regioselective intermolecular 1,2-aryl-aminoalkylation of alkenes by photoredox/nickel dual catalysis is described here. This three-component conjunctive cross-coupling is highlighted by its first application of primary alkyl radicals, which were not compatible in previous reports. The readily prepared α-silyl amines could be transferred to α-amino radicals by photo-induced single electron transfer step. The radical addition/cross-coupling cascade reaction proceeds under mild, base-free and redox-neutral conditions with good functional group tolerance, and importantly, provides an efficient and concise method for the synthesis of structurally valuable α-aryl substituted γ-amino acid derivatives motifs.

NITROGEN-CONTAINING ORGANOSILICON COMPOUNDS LXXXIX. SYNTHESIS AND CHROMATOGRAPHIC AND 13C, 15N, AND 29SI NMR-SPECTRAL INVESTIGATIONS OF PIPERAZINYLSILANES

Lukevits, E.,Liepin'sh, E.,Popova, E. P.,Shatts, V. D.,Belikov, V. A.

, p. 317 - 324 (2007/10/02)

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