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67372-96-7

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67372-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67372-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,7 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67372-96:
(7*6)+(6*7)+(5*3)+(4*7)+(3*2)+(2*9)+(1*6)=157
157 % 10 = 7
So 67372-96-7 is a valid CAS Registry Number.

67372-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3-propan-2-ylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-iso-propylsalicylaldehyde

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:67372-96-7 SDS

67372-96-7Relevant articles and documents

New water soluble bis-imidazolium salts with a saldach scaffold: Synthesis, characterization and in vitro cytotoxicity/bactericidal studies

Elshaarawy, Reda F.M.,Kheiralla, Zeinab H.,Rushdy, Abeer A.,Janiak, Christoph

, p. 110 - 122 (2014)

A series of water-soluble bis-imidazolium salts of the type H 2(iPr)2saldach(1,2-Me2Im +-X-)2 (4) and their mononuclear complexes [M(III)Cl{(iPr)2saldach(1,2-Me2Im +-X-)2}] (M = Mn, 5; Fe, 6), (X = Cl, a; PF6, b; BF4, c), where saldach = N,N′- bis(salicylidene)-(±)-trans-1,2-diaminocyclohexane, have been synthesized and characterized using elemental analysis, electronic, spectral, magnetic as well as conductometric methods and MALDI-TOF-, ESI-MS. All complexes possess a distorted square pyramidal coordination geometry with MN2O 2Cl chromophore, as revealed by the elemental, spectral and literature data. These salts have been evaluated for in vitro cytotoxicity against HepG-2 and MCF-7 cell lines. Among them, 4c (IC50 = 22.17 μM) exhibited potency against MCF-7. The bactericidal efficacy of 4a-c was screened against a panel of common pathogenic bacteria. Compound 4a was found to be the most potent antibacterial agent and could inhibit all the bacterial strains more effectively than standard antibiotics.

UHMWPE with short-chain branches synthesized by alkenyl substituted phenoxy–imine catalysts in ethylene polymerization

Wang, Yi,Fan, Hong,Li, Bo-Geng

, p. 3808 - 3818 (2016)

The alkenyl substituted phenoxy–imine complexes [2-C3H5-6-(2, 3, 5, 6-C6F4H-N?CH)C6H3O]2TiCl2 (C3H5=?CH2? CH?CH2 or ?CH?CH?

Ionic Sal-SG Schiff bases as new synergetic chemotherapeutic candidates: Synthesis, metalation with Pd(ii) and in vitro pharmacological evaluation

Elshaarawy, Reda F. M.,Mostafa, Tahia B.,Refaee, Ayaat A.,El-Sawi, Emtithal A.

, p. 68260 - 68269 (2015/09/01)

A series of novel N-(salicylidene)-sulfaguanidines (Sal-SG) bearing ionic liquid (IL) terminals (ILSSGH, 4a-f) have been synthesized by Schiff base condensation of IL-functionalized salicylaldehydes (ILSal, 3a-g) and sulfaguanidine (SG). Metalation trials of these ionic Schiff bases with palladium(ii) chloride affords the corresponding Pd(ii) complexes, [Pd(ii)(ILSSG)Cl(H2O)] (5a-g). Further, the antimicrobial profiles of the new compounds against a set of common pathogens have been described. Zone of inhibition (ZOI) and minimal inhibitory concentration (MIC) values revealed that most of the new compounds exhibited significant antibacterial and potential inhibitory activity against Staphylococcus aureus (S. aureus), and this activity is modulated by substituents attached to the ionic liquid core as well as the counter-ion.

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