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103619-04-1

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103619-04-1 Usage

General Description

The chemical "(3R,5R,6S)-3,5-dimethyl-6-[(2R)-pentan-2-yl]tetrahydro-2H-pyran-2-one" is a compound with a complex molecular structure. It is a tetrahydro-2H-pyran-2-one derivative with two methyl groups and a pentan-2-yl group attached to it. The stereochemistry of the molecule is specified by the (3R,5R,6S) configuration. (3R,5R,6S)-3,5-dimethyl-6-[(2R)-pentan-2-yl]tetrahydro-2H-pyran-2-one may have potential biological activities or pharmaceutical applications, but further research would be needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 103619-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103619-04:
(8*1)+(7*0)+(6*3)+(5*6)+(4*1)+(3*9)+(2*0)+(1*4)=91
91 % 10 = 1
So 103619-04-1 is a valid CAS Registry Number.

103619-04-1SDS

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 (3R,5R,6S)-3,5-dimethyl-6-[(2R)-pentan-2-yl]oxan-2-one

1.2 Other means of identification

Product number -
Other names (-)-Invictolide

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:103619-04-1 SDS

103619-04-1Downstream Products

103619-04-1Relevant articles and documents

Synthesis of (-)-Invictolide, the Pheromone Component of the Red Imported Fire Ant

Senda, Shuji,Mori, Kenji

, p. 1379 - 1384 (2007/10/02)

(-)-Invictolide was synthesized in 16 steps from 2-methylpentanal.

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