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135096-78-5

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135096-78-5 Usage

General Description

Hydroquinine 9-phenanthryl ether is a chemical compound that is derived from hydroquinone and phenanthrene. It is commonly used as a reagent in organic synthesis and as a precursor in the production of other organic compounds. The compound's structure consists of a hydroquinone moiety linked to a phenanthryl group. It has been shown to have potential applications in the pharmaceutical and agrochemical industries, as well as in the production of various materials. Its unique structure and properties make it a valuable and versatile chemical for use in a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 135096-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,9 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135096-78:
(8*1)+(7*3)+(6*5)+(5*0)+(4*9)+(3*6)+(2*7)+(1*8)=135
135 % 10 = 5
So 135096-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C34H34N2O2/c1-3-22-21-36-17-15-23(22)19-32(36)34(29-14-16-35-31-13-12-26(37-2)20-30(29)31)38-33-27-10-6-4-8-24(27)18-25-9-5-7-11-28(25)33/h4-14,16,18,20,22-23,32,34H,3,15,17,19,21H2,1-2H3/t22-,23?,32?,34-/m1/s1

135096-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(R)-[(2S,4S,5R)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-phenanthren-9-yloxymethyl]-6-methoxyquinoline

1.2 Other means of identification

Product number -
Other names O-(9-Phenanthryl)hydroquinine

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:135096-78-5 SDS

135096-78-5Upstream product

135096-78-5Downstream Products

135096-78-5Relevant articles and documents

A ligand structure-enantioselectivity relationship for the osmium-catalyzed asymmetric dihydroxylation of olefins

Ogino, Yasukazu,Chen, Hou,Manoury, Eric,Shibata, Tomoyuki,Beller, Matthias,Luebben, Doris,Sharpless, K. Barry

, p. 5761 - 5764 (2007/10/02)

The highest enantioselectivities to date for various olefins are obtained in the osmium-catalyzed asymmetric dihydroxylation using new 9-O-aromatic dihydroquinidine and dihydroquinine ligands. A ligand structure-enantioselectivity relationship (LSER) is developed, and representative results for quinine-based ligands are reported for the first time.

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