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503540-53-2

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503540-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503540-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,4 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 503540-53:
(8*5)+(7*0)+(6*3)+(5*5)+(4*4)+(3*0)+(2*5)+(1*3)=112
112 % 10 = 2
So 503540-53-2 is a valid CAS Registry Number.

503540-53-2SDS

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 1,4-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-1,4-diazacycloheptane

1.2 Other means of identification

Product number -
Other names -

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:503540-53-2 SDS

503540-53-2Downstream Products

503540-53-2Relevant articles and documents

Synthesis, characterization and crystal structure of a phenol-functionalized diazamesocyclic derivative with unexpected configuration

Guo, Ya-Mei,Du, Miao,Bu, Xian-He

, p. 191 - 196 (2003)

A bis-substituent diazamesocyclic compound containing bulky phenolic donor pendants, 1,4-bis(3-tert-butyl-5-methyl-2-hydroxybenzyl)-1,4-diazacycloheptane, has been prepared from 1,4-diazacycloheptane (DACH) and 2-tert-butyl-4-methylphenol by the Mannich reaction, and structurally characterized by NMR, IR and X-ray diffraction techniques. The crystal structure of the title compound reveals that 1,4-diazacycloheptane (DACH) ring is folded up into unusual chair configuration, and the two phenol pendants of the compound are in unexpected trans positions, which is different from those in the transition metal complexes of DACH and its derivatives. There exist intra-molecular O-H···N hydrogen bonds between the phenolic O atoms and the DACH N donors which stabilize the crystal structure.

Homopiperazine and piperazine complexes of ZrIV and Hf IV and their application to the ring-opening polymerisation of lactide

Hancock, Stuart L.,Mahon, Mary F.,Kociok-Kohn, Gabriele,Jones, Matthew D.

experimental part, p. 4596 - 4602 (2011/12/01)

In this paper we describe the preparation and characterisation, by single-crystal X-ray diffraction, of twelve ZrIV/HfIV complexes based on piperazine or homopiperazine salan ligands. With the piperazine ligands, a mixture of species

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