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2-Heptanone, 7-hydroxy-, also known as 7-Hydroxy-2-heptanone or 7-Hydroxyheptanal, is an organic compound with the chemical formula C7H14O2. It is a colorless liquid with a molecular weight of 130.19 g/mol. 2-Heptanone, 7-hydroxy- is characterized by the presence of a hydroxyl group (-OH) at the 7th carbon atom and a ketone group (C=O) at the 2nd carbon atom in a heptane chain. 2-Heptanone, 7-hydroxy- is an important intermediate in the synthesis of various pharmaceuticals, fragrances, and other organic compounds. It is also used as a solvent and a reagent in chemical reactions. Due to its reactive nature, it is essential to handle 2-Heptanone, 7-hydroxy- with care, following proper safety protocols.

5070-59-7

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5070-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5070-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5070-59:
(6*5)+(5*0)+(4*7)+(3*0)+(2*5)+(1*9)=77
77 % 10 = 7
So 5070-59-7 is a valid CAS Registry Number.

5070-59-7SDS

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 7-hydroxyheptan-2-one

1.2 Other means of identification

Product number -
Other names 1-hydroxyheptan-6-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:5070-59-7 SDS

5070-59-7Upstream product

5070-59-7Downstream Products

5070-59-7Relevant academic research and scientific papers

Efficient and selective oxidation of methyl substituted cycloalkanes by heterogeneous methyltrioxorhenium-hydrogen peroxide systems

Bianchini, Gianluca,Crucianelli, Marcello,Canevali, Carmen,Crestini, Claudia,Morazzoni, Franca,Saladino, Raffaele

, p. 12326 - 12333 (2006)

Polymer-supported methyltrioxorhenium (MTO) systems are efficient catalysts for the oxidative functionalisation of cyclohexane and cyclopentane derivatives with H2O2 as oxygen donor. Using poly(4-vinyl)pyridine and poly(4-vinyl)pyridine-N-oxide as MTO supports, cycloalkanol, cycloalkanediol, cycloalkanone and ω-hydroxy methyl ketone derivatives were obtained in different yields depending on the experimental conditions. Interestingly, cycloalkane dimers were selectively recovered in acceptable to good yields when the oxidation was performed with polystyrene-microencapsulated MTO catalyst. The EPR investigation suggests that the homolytic cleavage of the CH3-Re bond with formation of CH3{radical dot} radicals occurs inside the polystyrene capsule, indicating a possible role of methyl radical in the cycloalkane dimerisation pathway.

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