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39192-51-3

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39192-51-3 Usage

General Description

1-(3 5-DIMETHOXYPHENYL)HEPTAN-1-ONE 96 refers to a specialized chemical compound that contains a 7-carbon chain (HEPTAN-1-ONE) functional group with a compound 3,5-DIMETHOXYPHENYL at the first carbon. The presence of the Methoxy groups at positions 3 and 5 on the phenyl ring indicates that it is dimethoxyphenyl. It falls under the category of organic compounds more specifically, aromatic ketones. Detailed information about its properties like melting point, boiling point, solubility, toxicity, or how it reacts with other substances might not be readily available as it appears to be a specialized or less common compound. Purity of this compound is denoted by the number 96, implying it is 96% pure, often used in research and development fields.

Check Digit Verification of cas no

The CAS Registry Mumber 39192-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39192-51:
(7*3)+(6*9)+(5*1)+(4*9)+(3*2)+(2*5)+(1*1)=133
133 % 10 = 3
So 39192-51-3 is a valid CAS Registry Number.

39192-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-Dimethoxyphenyl)heptan-1-one

1.2 Other means of identification

Product number -
Other names 1-(3,5-dimethoxyphenyl)heptan-1-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:39192-51-3 SDS

39192-51-3Relevant articles and documents

Synthesis of functionalized cannabinoids

Harrington, Paul E.,Stergiades, Ioanna A.,Erickson, Joy,Makriyannis, Alexandros,Tius, Marcus A.

, p. 6576 - 6582 (2007/10/03)

An effective synthesis of tricyclic, nonclassical cannabinoids has been developed on the basis of a cation-olefin cyclization that forms the two nonaromatic rings with the desired stereochemistry in a single step.

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