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24596-41-6

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24596-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24596-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24596-41:
(7*2)+(6*4)+(5*5)+(4*9)+(3*6)+(2*4)+(1*1)=126
126 % 10 = 6
So 24596-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N3/c1-18(2,3)14-6-8-15(9-7-14)19-20-16-10-12-17(13-11-16)21(4)5/h6-13H,1-5H3/b20-19+

24596-41-6SDS

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 4-[(4-tert-butylphenyl)diazenyl]-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-tert.-Butyl-4'-N,N-dimethylaminoazobenzol

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:24596-41-6 SDS

24596-41-6Downstream Products

24596-41-6Relevant articles and documents

Juri,Bartsch

, p. 143 (1979)

Host-Guest Complexation. 41. Preorganization of a Host Enhances Its Binding of Aryldiazonium Salts

Cram, Donald J.,Doxsee, Kenneth M.

, p. 5068 - 5071 (1986)

Synthetic host 1, a spherand comprised of cyclic urea and aryl ether units, has been designed and examined.It displays markedly superior binding of aryldiazonium tetrafluoroborate salts over previously reported complexing agents.Qualitative experiments indicate a higher degree of stabilization of complexed diazonium salts toward thermal decomposition and azo dye formation than is given by 18-crown-6.Quantitative infrared studies yield an approximate binding free energy of -5.9 kcal mol-1 for the complexation of p-(CH3)3CC6H4N2BF4 by 1 in ClCH2CH2Cl at 25 deg C, appr eciably higher than the -3.6 kcal mol-1 determined for 18-crown-6 under identical conditions.Addition of an aqueous solution of Na2CO3 to a colorless solution of CH2Cl2 containing C6H5N(CH3)2 and 1 complexed to p-(CH3)3CC6H4N2BF4 instantaneously released the aryldiazonium ion which coupled to form the azxo dye.The alkali metal salts bind 1 much more strongly than does the aryldiazonium salt.Thus the Na+ ion acts as a trigger for dye formation, the system as a whole acting as an indicator for the presence of alkali metal ions.

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