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35345-72-3

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35345-72-3 Usage

Uses

11-Hydroxyundecan-2-one is an intermediate in the synthesis of 1,2-Benzenedicarboxylic Acid 1-(10-Hydroxyundecyl) Ester (B488585), a as potential biomarker for assessment of diundecyl phthalate exposure in human liver microsome.

Check Digit Verification of cas no

The CAS Registry Mumber 35345-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35345-72:
(7*3)+(6*5)+(5*3)+(4*4)+(3*5)+(2*7)+(1*2)=113
113 % 10 = 3
So 35345-72-3 is a valid CAS Registry Number.

35345-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-10-undecanone

1.2 Other means of identification

Product number -
Other names 11-Hydroxyundecan-2-one

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:35345-72-3 SDS

35345-72-3Relevant articles and documents

Discovery and Comparison of Homogeneous Catalysts in a Standardized HOT-CAT Screen with Microwave-Heating and qNMR Analysis: Exploring Catalytic Hydration of Alkynes

Brunner, Andreas,Hintermann, Lukas,Milzarek, Tobias M.,Schreyer, Matthias,Wegmann, Marcus

, (2019)

A HOT-CAT (homogeneous thermal catalysis) screen using microwave-heating and quantitative NMR (qNMR) analysis has been developed for identification and comparison of catalyst activity in homogeneous metal-based catalysis. The hydration of terminal alkynes to ketones or aldehydes served as a model reaction in this proof-of-concept study. Key aspects of the screen are the use of a high-temperature setting (e. g., 160 °C) at a fixed, short reaction time (e. g., 15 min) for all samples. Analysis of crude reaction mixtures by a standardized, quantitative 1H NMR protocol gives a comprehensive picture of catalyst chemo- and regioselectivity, which permits broad comparisons and the discovery of non-target reactivity. For catalytic alkyne hydration, data for 105 runs involving 81 catalyst systems with 15 different metals is presented. The activity of all established catalyst systems was reproduced, and new catalyst systems with Markovnikov hydration selectivity were discovered and applied to preparative runs, namely Cu2O?CSA (CSA=camphorsulfonic acid), Co(OAc)2?tetraphenylporphyrin?CSA and [IrCl(COD)]?CSA.

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