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Hexanedioic acid bis(cholest-5-en-3β-yl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23394-15-2

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23394-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23394-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23394-15:
(7*2)+(6*3)+(5*3)+(4*9)+(3*4)+(2*1)+(1*5)=102
102 % 10 = 2
So 23394-15-2 is a valid CAS Registry Number.

23394-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dicholesteryl adipate

1.2 Other means of identification

Product number -
Other names Hexanedioic acid bis-[(3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] ester

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:23394-15-2 SDS

23394-15-2Downstream Products

23394-15-2Relevant academic research and scientific papers

Direct synthesis of adipic acid esters via palladium-catalyzed carbonylation of 1,3-dienes

Yang, Ji,Liu, Jiawang,Neumann, Helfried,Franke, Robert,Jackstell, Ralf,Beller, Matthias

, p. 1514 - 1517 (2020/01/08)

The direct carbonylation of 1,3-butadiene offers the potential for a more cost-efficient and environmentally benign route to industrially important adipic acid derivatives. However, owing to the complex reaction network of regioisomeric carbonylation and isomerization pathways, a selective practical catalyst for this process has thus far proven elusive. Here, we report the design of a pyridyl-substituted bidentate phosphine ligand (HeMaRaphos) that, upon coordination to palladium, catalyzes adipate diester formation from 1,3-butadiene, carbon monoxide, and butanol with 97% selectivity and 100% atom-economy under industrially viable and scalable conditions (turnover number > 60,000). This catalyst system also affords access to a variety of other di- and triesters from 1,2- and 1,3-dienes.

Thermal and optical properties of chiral twin liquid crystalline bis(cholesteryl) alkanedioates

Marcelis, Antonius T. M.,Koudijs, Arie,Sudhoelter, Ernst J. R.

, p. 1469 - 1472 (2007/10/03)

The thermal and optical properties of a series of bis(cholesteryl) alkanedioates were investigated. The melting points, the cholesteric to isotropic transition temperatures, the entropy changes at this temperature and the selective reflection wavelengths of the cholesteric phase all exhibit an odd-even effect as a function of spacer length. This is attributed to a difference in the ordering of the cholesteric phase as a function of the parity of the spacer. Because the properties of the members of the series with a short spacer could not be measured for several reasons, their properties were also determined as a 5 wt% solution in a cholesteric host. A similar odd-even influence on the cholesteric to isotropic transition temperatures and the optical properties of the host was observed as for the pure compounds. The influence on the properties of the host is stronger for compounds with a short spacer than for compounds with a longer spacer.

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