cas 6920-24-7, 1,2-Hexadecanediol | Articles data ｜lookchem

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6920-24-7

Articles about 6920-24-7Total 7 be found

Article title
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Weiss
p. 1576
(1965)
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Cram,Abell
p. 1179,1180
(1955)
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Ring opening of a fatty epoxide by diethylacetamido malonate in basic medium by phase transfer catalysis or under microwave irradiation
A fatty epoxide (tetradecyl-oxirane) is reacted with diethyl acetamidomalonate in basic medium, with or without solvent under solid-liquid phase transfer catalysis with LiCl, or under microwave irradiation on supported reagents (KF/Al2O3/LiCl). The main product is a lactone which is formed after epoxide ring opening and subsequent cyclisation. We put here into evidence, for the first time, the conjugated advantages of 'dry media' reactions, lithium salt effects and microwave irradiation.
Abenhaim,Loupy,Mahieu,Semeria
p. 1809 - 1816
(1994)
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Sheehan,Bose
p. 4957
(1952)
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Total synthesis of (-)-goniotrionin
A stereoselective total synthesis of the reported structure of goniotrionin (4) has been accomplished. The key steps involved the opening of a chiral epoxide, a highly diastereoselective Mukaiyama aerobic oxidative cyclization, a selective 1,2-syn Mukaiyama aldol reaction, and a Noyori reduction.
Dias, Luiz C.,Ferreira, Marco A. B.
experimental part
p. 4046 - 4062
(2012/06/29)

Catalysts/cosolvents and general acid catalysts for acceleration of the hydrolysis of osmate(VI) esters
New catalysts/cosolvents as hydrolysis aids and the properties of the catalyst/cosolvent that effect the efficiency of the hydrolysis aid for the hydrolysis of osmate(VI) esters of aliphatic olefins are presented. Also, the effect of pH of the reaction media on the specific and general acid-catalysed hydrolysis of osmate(VI) esters of conjugated aromatic olefins is presented.
Junttila, Mikko H.,Hormi, Osmo E.O.
supporting information; scheme or table
p. 3430 - 3432
(2010/09/05)

DERMATOLOGICAL COMPOSITIONS AND METHODS
Disclosed are methods and compositions for regulating the melanin content of mammalian melanocytes; regulating pigmentation in mammalian skin, hair, wool or fur; treating or preventing various skin and proliferative disorders; by administration of various compounds, including alcohols, diols and/or triols and their analogues.
-
(2008/06/13)

Treatment of neurodegenerative diseases
Disclosed are methods for increasing the differentiation of mammalian neuronal cells for purposes of treating neurodegenerative diseases or nerve damage by administration of various compounds including alcohols, diols and/or triols and their analogues.
-
(2008/06/13)

Treatment of diseases mediated by the nitric oxide/cGMP/protein kinase G pathway
Disclosed are methods and compositions for stimulating cellular nitric oxide (NO) synthesis, cyclic guanosine monophosphate levels (cGMP), and protein kinase G (PKG) activity for purposes of treating diseases mediated by deficiencies in the NO/cGMP/PKG signal transduction pathway, by administration of various compounds including alcohols, diols and/or triols and their analogues.
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(2008/06/13)

1,y Dihydroxy paraffins
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Akal Baser
p. 524 - 526
(2007/10/05)

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Chemical Properties

Melting Point: 68-72 °C(lit.)
Boiling Point: 356.1oC at 760 mmHg
Flash Point:183oC
Density: 0.897g/cm3
Vapor Pressure: 1.69E-06mmHg at 25°C
Refractive Index: 1.4731 (estimate)
PKA: 14.45±0.20(Predicted)
BRN: 1722206
PSA: 40.46000
LogP: 4.43080

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