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1,3-Nonanediol, 3-methyl-, 1-(4-methylbenzenesulfonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68329-37-3

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68329-37-3 Usage

Common Uses

Lubricants, plasticizers, and surfactants

Production Method

Esterification of 1,3-nonanediol with 4-methylbenzenesulfonic acid

Physical Appearance

White to off-white powder

Solubility

Soluble in water and organic solvents

Functionality

Acts as an emulsifying agent

Industrial Applications

Wide range of industrial and commercial applications

Toxicity

Relatively low toxicity

Environmental Impact

Environmentally friendly

Derivative of

Nonanediol

Check Digit Verification of cas no

The CAS Registry Mumber 68329-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68329-37:
(7*6)+(6*8)+(5*3)+(4*2)+(3*9)+(2*3)+(1*7)=153
153 % 10 = 3
So 68329-37-3 is a valid CAS Registry Number.

68329-37-3Downstream Products

68329-37-3Relevant academic research and scientific papers

The Synthesis of 8,10,12-Triazaprostaglandin Analogues: 1,2,4-Triazolidine-3,5-dione Derivatives

Adams, David R.,Barnes, Alan F.,Cassidy, Frederick,Thompson, Mervyn

, p. 2061 - 2068 (2007/10/02)

In the search for active, more selective prostaglandin analogues, the synthesis of 8,10,12-triazaprostaglandin analogues has been achieved from readily available 4-methyl-1,2,4-triazolidine-3,5-dione.The general approach involved introduction of the α- and ω-side-chain as entire units by step-wise N-alkylation.The problems encountered with this approach of competing N- and O-mono- and di-alkylation were overcome, eventually, such that judicious choice of the initial mono-N-alkylation step enabled the synthesis of analogues incorporating wide variations in the α- and ω-side-chain.Important structural modifications included introduction of unsaturation into the α-side-chain at the 5,6-position and of methyl groups into the ω-side-chain at the 15- and 16-position as exemplified by the synthesis of 1--2-(3-hydroxy-3,4-dimethyloctyl)-4-methyl-1,2,4-triazolidine-3,5-dione (19).The stable triazaprostaglandin analogues were synthesized as racemic compounds but, nevertheless, compound (19) possessed bronchodilator activity of a similar order to that of the natural prostaglandins PGE1 and PGE2.

1,2-Disubstituted oxo triazolidine

-

, (2008/06/13)

Compounds of the formula (I): STR1 wherein n is 3 to 5; Y is --CH2 --CH2, --CH=CH-- or C C--; L is O or S; R1 is C1-4 alkyl; R2 is hydrogen, C1-4 alkyl or phenyl; R3 is hydroxy o

SYNTHESIS OF 12-AZAPROSTACYCLIN ANALOGUES

Cassidy, F.,Moore, R. W.,Wootton, G.,Baggaley, K. H.,Geen, G. R.,et. al.

, p. 253 - 256 (2007/10/02)

Synthetic routes for the preparation of 12-azaprostacyclin analogues are described.

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