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86100-84-7

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86100-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86100-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,0 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86100-84:
(7*8)+(6*6)+(5*1)+(4*0)+(3*0)+(2*8)+(1*4)=117
117 % 10 = 7
So 86100-84-7 is a valid CAS Registry Number.

86100-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-dipropoxy-2,2'-dihydroxy-α,α'-dimethylbenzalazine

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:86100-84-7 SDS

86100-84-7Downstream Products

86100-84-7Relevant articles and documents

The π-π interactions enhanced in salicylaldimines and salicylaldazines

Kuo, Hsiu-Ming,Hsu, Yu-Te,Wang, Yi-Wen,Lee, Gene-Hsiang,Lai, Chung K.

, p. 7729 - 7738 (2015/09/07)

Four new series of salicylaldazines 1 and salicylaldimines 2-4 were prepared, characterized and their mesomorphic properties were studied. The structures of all compounds were identified and confirmed by spectroscopic techniques such as 1H, 13C NMR, MS and elemental analysis. Three single crystallographic structures of compounds 1a (n=3, 6) and 2 (n=3) were determined by X-ray analysis in order to correlate the molecular structures with the formation of mesophases. Crystallographic data indicated that the better mesomorphic properties might be controlled by CH-π, π-π or/and H-bonds in such system. Except for crystalline compounds 4, all other compounds 1-3 showed mesomorphic behavior of nematic, smectic A or/and smectic C phases, which were characterized by differential scanning calorimetry, optical polarizing microscope and X-ray diffraction experiments. All compounds 1-4 showed yellow-green photoluminescence in THF occurred at 519-521 nm.

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