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Cyclopentadecanone, 5-hydroxy-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85037-96-3

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85037-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85037-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85037-96:
(7*8)+(6*5)+(5*0)+(4*3)+(3*7)+(2*9)+(1*6)=143
143 % 10 = 3
So 85037-96-3 is a valid CAS Registry Number.

85037-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-3-methylcyclopentadecan-1-one

1.2 Other means of identification

Product number -
Other names Cyclopentadecanone,5-hydroxy-3-methyl

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:85037-96-3 SDS

85037-96-3Downstream Products

85037-96-3Relevant academic research and scientific papers

Method for preparing chiral musk ketone

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Paragraph 0041; 0042, (2021/02/09)

A method for preparing chiral muscone is provided. 3-methyl-cyclopentadecane-1,5-dione is adopted as an initial raw material, chiral rhodium and a Br nsted acid are adopted as catalysts, hydrogen is adopted as a reductant, and a chiral muscone product is synthesized in a one-pot manner through asymmetric hydrogenation, hydrogenolysis and other reactions. The method is short and simple in route, high in total yield, low in generation of three types of waste and suitable for industrial production of the chiral muscone.

Method for the preparation of compounds having a 16-oxabicyclo[10.3.1]pentadecene scaffold and the subsequent products thereof

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Paragraph 0234, (2019/01/04)

The present invention relates to a method for preparing compounds having a 16-oxabicyclo[10.3.1]pentadecene skeleton, specifically 14-methyl-16-oxabicyclo[10.3.1]pentadecenes, and conversion products thereof.

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