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1-Aza-2,5-disilacyclopentane, 1-[(3-bromophenyl)methyl]-2,2,5,5-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222729-15-9

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222729-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222729-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,7,2 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 222729-15:
(8*2)+(7*2)+(6*2)+(5*7)+(4*2)+(3*9)+(2*1)+(1*5)=119
119 % 10 = 9
So 222729-15-9 is a valid CAS Registry Number.

222729-15-9SDS

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 1-(-3-bromobenzyl)-2,2,5,5-tetramethyl-1,2,5-azadisilolidine

1.2 Other means of identification

Product number -
Other names 1-(3-bromobenzyl)-2,2,5,5-tetramethyl-1,2,5-azadisilolidine

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:222729-15-9 SDS

222729-15-9Downstream Products

222729-15-9Relevant academic research and scientific papers

PREPARATIONS OF META-IODOBENZYLGUANIDINE AND PRECURSORS THEREOF

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Paragraph 0140, (2021/06/25)

The present disclosure provides purified forms of iobenguane and preparations of a precursor to iobenguane, such as a polymer, the polymer comprising a monomer of formula (I) or a pharmaceutically acceptable salt thereof, the preparation comprising leacha

Transition-state stabilization by a secondary substrate-ligand interaction: A new design principle for highly efficient transition-metal catalysis

Smejkal, Tomas,Gribkov, Denis,Geier, Jens,Keller, Manfred,Breit, Bernhard

supporting information; experimental part, p. 2470 - 2478 (2010/06/17)

A library of monodentate phosphane ligands, each bearing a guanidine receptor unit for carboxylates, was designed. Screening of the library gave some excellent catalysts for regioselective hydroformylation of ss,γ- unsaturated carboxylic acids. A terminal alkene, but-3-enoic acid, was hydroformylated with a linear/branched (l/b) regioselectivity up to 41. An internal alkene, pent-3-enoic acid was hydroformylated with regioselectivity up to 18:1. Further substrate selectivity (e.g., acid vs. methyl ester) and reaction site selectivity (monofunctionalization of 2- vinylhept-2-enoic acid) were also achieved. Exploration of the structure-activity relationship and a practical and theoretical mechanistic study gave us an insight into the nature of the supramolecular guanidinium-carboxylate interaction within the catalytic system. This allowed us to identify a selective transition-state stabilization by a secondary substrate-ligand interaction as the basis for catalyst activity and selectivity.

Methods for purifying radiolabelled compounds

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Page/Page column 13; 22, (2008/06/13)

One aspect of the present invention relates to a method of purifying radiolabelled compounds comprising a) loading onto a fluorous polymer a radiolabelled compound precursor comprising a fluoroalkyl tin moiety; b) reacting the radiolabelled compound precursor with a radiolabel delivering compound to give a radiolabelled compound, wherein the fluoroalkyl tin moiety is replaced by a radiolabel; and c) eluting the radiolabelled compound from the fluorous polymer.

Preparation of radiolabelled haloaromatics via polymer-bound intermediates

-

, (2008/06/13)

According to a first aspect of the invention, a process is disclosed for the preparation of radiolabelled haloaromatic compounds. According to a second aspect of the invention, intermediate precursor insoluble polymer compounds used in the preparation of

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