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1,16-Hexadecanediol, bis(4-methylbenzenesulfonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73992-43-5

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73992-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73992-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73992-43:
(7*7)+(6*3)+(5*9)+(4*9)+(3*2)+(2*4)+(1*3)=165
165 % 10 = 5
So 73992-43-5 is a valid CAS Registry Number.

73992-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name O,O'-ditosyl-1,16-hexadecanediol

1.2 Other means of identification

Product number -
Other names 1,16-Hexadecandiol-bis-p-toluolsulfonat

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:73992-43-5 SDS

73992-43-5Relevant academic research and scientific papers

Synthesis of 13C-labelled cutin and suberin monomeric dicarboxylic acids of the general formula HO213C-(CH2)n-13CO2H (n = 10, 12, 14, 16, 18, 20, 22, 24, 26, 28)

Schink, Carina,Spielvogel, Sandra,Imhof, Wolfgang

, p. 14 - 29 (2020/11/30)

13C-labeled dicarboxylic acids HO213C-(CH2)n-13CO2H (n = 10, 12, 14, 16, 18, 20, 22, 24, 26, 28) have been synthesized as internal standards for LC-MS and GC-MS analysis of cutin and suberin monomer degradation by soil-based microorganisms. Different synthetic strategies had to be applied depending on the chain length of the respective synthetic target and because of economic considerations. 13C-labels were introduced by nucleophilic substitution of a suitable leaving group with labelled potassium cyanide and subsequent hydrolysis of the nitriles to produce the corresponding dicarboxylic acids. All new compounds are characterized by GC/MS, IR, and NMR methods as well as by elemental analysis.

Synthesis and Characterization of Constitutionally Isomeric Oriented Calix[6]arene-Based Rotaxanes

Zanichelli, Valeria,Ragazzon, Giulio,Arduini, Arturo,Credi, Alberto,Franchi, Paola,Orlandini, Guido,Venturi, Margherita,Lucarini, Marco,Secchi, Andrea,Silvi, Serena

, p. 1033 - 1042 (2016/03/01)

Oriented rotaxanes composed of tris(N-phenylureido)calix[6]arene wheel 1 and N,N′-dialkyl viologen-based axles were synthesized in which the span between the diphenylacetyl stoppers at the wheel upper and lower rim and the bis-pyridinium cation portion of

Synthesis of Hsp90 inhibitor dimers as potential antitumor agents

Muranaka, Kazuhiro,Sano, Akiko,Ichikawa, Satoshi,Matsuda, Akira

, p. 5862 - 5870 (2008/12/21)

Structure-based drug design was used to systematically synthesize PU3-dimers. The cytotoxicity of PU3 dimers 6 against breast cancer cell lines was evaluated, and their potency increased as the length of the bridging linker increased. Among the compounds

Bis-imidazoles as molecular probes for peripheral sites of the zinc endopeptidase of botulinum neurotoxin serotype A

Merino, Isidro,Thompson, Jason D.,Millard, Charles B.,Schmidt, James J.,Pang, Yuan-Ping

, p. 3583 - 3591 (2007/10/03)

Botulinum neurotoxin serotype A (BoNTA) is highly toxic, and its antidote is currently unavailable. The essential light-chain subunit of BoNTA is a zinc endopeptidase that can be used as a target for developing antidotes. However, the development of high-

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