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17619-06-6

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17619-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17619-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17619-06:
(7*1)+(6*7)+(5*6)+(4*1)+(3*9)+(2*0)+(1*6)=116
116 % 10 = 6
So 17619-06-6 is a valid CAS Registry Number.

17619-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-6-[(3-tert-butyl-2-hydroxy-5-methylphenyl)-phenylmethyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names 6,6'-Di-tert-butyl-4,4'-dimethyl-2,2'-benzyliden-di-phenol

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:17619-06-6 SDS

17619-06-6Downstream Products

17619-06-6Relevant articles and documents

2. 2' - Benzyl - different substituted [...] ethyl aluminum compound and its preparation method

-

Paragraph 0015-0016, (2018/09/29)

The invention relates to a 2, 2' - benzyl - different substituted [...] ethyl aluminum compound and its preparation method, its preparation method is as follows: the benzaldehyde and containing different substituent of the phenol to the molar ratio of 1:2

Optimization of asymmetric catalysts using achiral ligands: metal geometry-induced ligand asymmetry.

Davis,Balsells,Carroll,Walsh

, p. 2161 - 2164 (2007/10/03)

[reaction: see text] Traditionally, asymmetric catalysts have been optimized by modification of resolved chiral ligands. In this Letter, we optimize the asymmetric addition of diethylzinc to aldehydes by modification of achiral methylene bis(phenol) ligands. Upon coordination of the substrate, the achiral ligand becomes asymmetric, a concept termed Metal Geometry-Induced Ligand Asymmetry. The enantioselectivity of the catalyst formed from a single resolved ligand and several achiral ligands ranged from 9% (R) to 83% (S).

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