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9-oxabicyclo[6.1.0]nonan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

45828-32-8

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45828-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 45828-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,8,2 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 45828-32:
(7*4)+(6*5)+(5*8)+(4*2)+(3*8)+(2*3)+(1*2)=138
138 % 10 = 8
So 45828-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c9-6-4-2-1-3-5-7-8(6)10-7/h6-9H,1-5H2

45828-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-oxabicyclo[6.1.0]nonan-7-ol

1.2 Other means of identification

Product number -
Other names EINECS 256-247-1

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:45828-32-8 SDS

45828-32-8Upstream product

45828-32-8Downstream Products

45828-32-8Relevant academic research and scientific papers

Epoxidation with Ti(OSiMe3)4: A homogeneous model mimicking titania-silica mixed oxides?

Beck, Carsten,Mallat, Tamas,Baiker, Alfons

, p. 1284 - 1289 (2003)

Ti(OSiMe3)4 is an active homogeneous catalyst for the epoxidation of allylic alcohols under mild conditions using tert-butyl hydroperoxide as oxidant in an apolar solvent. It affords an average turnover frequency of up to 1470 h-1 and 100% regioselectivity (geraniol) or 100% cis-selectivity (cyclohexenol). UV-Vis measurements indicate that the ability of substrates to coordinate to the catalyst determines the reaction rate and stereoselectivity. This is the likely explanation for the poor or completely missing reactivity of substrates possessing no OH function (cyclohexene, methoxycyclohexene) and also for the substrate-dependent effect of water in the system. Ti(OSiMe3)4 is suggested to be a good soluble homogeneous model catalyst mimicking the highly active isolated tetrahedral Ti sites in (silylated) titania-silica mixed oxides.

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