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51152-11-5

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51152-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51152-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,5 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51152-11:
(7*5)+(6*1)+(5*1)+(4*5)+(3*2)+(2*1)+(1*1)=75
75 % 10 = 5
So 51152-11-5 is a valid CAS Registry Number.

51152-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-ISOPINOCAMPHEOL

1.2 Other means of identification

Product number -
Other names -

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:51152-11-5 SDS

51152-11-5Relevant articles and documents

Visible-Light-Mediated Aerobic Oxidation of Organoboron Compounds Using in Situ Generated Hydrogen Peroxide

Weng, Wei-Zhi,Liang, Hao,Zhang, Bo

supporting information, p. 4979 - 4983 (2018/08/24)

A simple and general visible-light-mediated oxidation of organoboron compounds has been developed with rose bengal as the photocatalyst, substoichiometric Et3N as the electron donor, as well as air as the oxidant. This mild and metal-free protocol shows a broad substrate scope and provides a wide range of aliphatic alcohols and phenols in moderate to excellent yields. Notably, the robustness of this method is demonstrated on the stereospecific aerobic oxidation of organoboron compounds.

Biology-oriented synthesis of a withanolide-inspired compound collection reveals novel modulators of hedgehog signaling

venda, Jakub,Sheremet, Michael,Kremer, Lea,Maier, Luk,Ziegler, Slava,Kumar, Kamal,Waldmann, Herbert,Bauer, Jonathan O.,Strohmann, Carsten

supporting information, p. 5596 - 5602 (2015/06/01)

Biology-oriented synthesis employs the structural information encoded in complex natural products to guide the synthesis of compound collections enriched in bioactivity. The trans-hydrindane dehydro-δ-lactone motif defines the characteristic scaffold of the steroid-like withanolides, a plant-derived natural product class with a diverse pattern of bioactivity. A withanolide-inspired compound collection was synthesized by making use of three key intermediates that contain this characteristic framework derivatized with different reactive functional groups. Biological evaluation of the compound collection in cell-based assays that monitored biological signal-transduction processes revealed a novel class of Hedgehog signaling inhibitors that target the protein Smoothened. BIOS delivers a collection of compounds with the trans-hydrindane dehydro-δ-lactone scaffold, which are based on the withanolide natural products, in a stereoselective fashion. A biological investigation of the compounds revealed novel and potent inhibitors of the Hedgehog signaling pathway, which bind to the protein Smoothened.

Use of immobilized transition metal complexes as recyclable catalysts for oxidation reactions with hydrogen peroxide as oxidant

Islam, Sk Manirul,Mobarok, Manir,Mondal, Paramita,Roy, Anupam Singha,Salam, Noor,Hossain, Dildar,Mondal, Sanchita

experimental part, p. 97 - 107 (2012/09/22)

A tetradentate Schiff base (teta), obtained from triethylenetetramine and salicylaldehyde, has been covalently bonded to divinylbenzene cross-linked chloromethylated polystyrene. This chelating ligand, abbreviated as PS-teta (PS = polymeric support), reacts with metal chlorides (Cu2+, Co 2+, and Ni2+) in methanol to give polymerbound transition metal complexes, PS-Cu(II)teta/(Cat-1), PS-Ni(II)teta/(Cat-2), and PS-Co(II)teta/(Cat-3), formation of which has been established by various physiochemical methods and spectroscopic techniques. The catalytic potential of these materials has been tested for the oxidation of various alkenes, alkanes, alcohols, and thioethers in the presence of 30% H2O2 as an oxidant. At the same time, these catalysts are very stable and could be reused in oxidation reactions for more than five times without noticeable loss of their catalytic activity. Springer Science+Business Media B.V. 2011.

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