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2-THIOANISOLEMAGNESIUM BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99346-84-6

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99346-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99346-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99346-84:
(7*9)+(6*9)+(5*3)+(4*4)+(3*6)+(2*8)+(1*4)=186
186 % 10 = 6
So 99346-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7S.BrH.Mg/c1-8-7-5-3-2-4-6-7;;/h2-5H,1H3;1H;/q;;+1/p-1/rC7H7BrMgS/c1-10-7-5-3-2-4-6(7)9-8/h2-5H,1H3

99346-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,methylsulfanylbenzene,bromide

1.2 Other means of identification

Product number -
Other names 2-Thioanisolemagnesium bromide 0.5 M in Tetrahydrofuran

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:99346-84-6 SDS

99346-84-6Relevant academic research and scientific papers

OLIGOMERISATION OF ETHYLENE TO MIXTURES OF 1-HEXENE AND 1-OCTENE

-

Page/Page column 33-34, (2014/12/09)

A process for the otigomerisation of ethylene to predominantly 1-hexene or 1-octene or mixtures of 1-hexene and 1-octene includes contacting ethylene with a catalyst under ethylene oligomerisation conditions. The catalyst comprises a source of chromium, a diphosphine ligating compound, and optionally an activator. The diphosphine ligating compound includes at least one optionally substituted fused cyclic structure including at least two rings, the optionally substituted fused cyclic structure including a 5- to 7- membered aromatic first ring bonded to a phosphorus atom, the aromatic first ring being fused to a 4- to 8-membered heterocyclic second ring, the heterocyclic second ring including a heteroatom which is separated by two ring atoms along the shortest connecting path from the phosphorous atom that is bonded to the first aromatic ring.

Phosphororganische Verbindungen 106. Die Synthese Optisch Aktiver Tertiaerer Phosphine und Phosphinoxide mit Ortho-Substituierten Arylliganden

Horner, L.,Simons, G.

, p. 77 - 90 (2007/10/02)

Compounds of the type C6H5Y (Y=OR, -NMe2), are lithiated with n-butyllithium (n-BuLi) in the ortho-position according (1) and transformed by special reactions to compounds of the type I and II. The representatives 7-22 of the type I with Y=OR ar

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