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2380-27-0

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2380-27-0 Usage

Chemical Properties

Light Brown Solid

Uses

Methyl 12-oxooctadecanoate was used in preparation of methyl hexahydro-3-hexyl-6-thioxo-1,2,4,5-tetrazine-3-undecanoate, hexahydrothioxotetrazine fatty derivative, via reaction with thiocarbohydrazide.

General Description

Methyl 12-oxooctadecanoate is a long chain keto fatty acid and its reaction with hydrazoic acid was studied.

Check Digit Verification of cas no

The CAS Registry Mumber 2380-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2380-27:
(6*2)+(5*3)+(4*8)+(3*0)+(2*2)+(1*7)=70
70 % 10 = 0
So 2380-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h3-17H2,1-2H3

2380-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 12-OXOOCTADECANOATE

1.2 Other means of identification

Product number -
Other names Methyl 12-ketostearate

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:2380-27-0 SDS

2380-27-0Relevant articles and documents

Synthesis, Characterisation, and Transformations of a Lipid Cyclic Peroxide

Bascetta, Emanuele,Gunstone, Frank D.,Scrimgeour, Charles M. S.

, p. 2199 - 2206 (2007/10/02)

Photosensitised oxidation of (9E,11E)-methyl octadeca-9,11-dienoate gave an unsaturated cyclic peroxide (epidioxide) in high yield.This was characterised spectroscopically.The peroxide underwent facile rearrangement to a furanoid ester under a variety of reaction conditions.Catalytic reduction of the unsaturated peroxide cleaved the O-O bond.Bromination and epoxidation gave dibromo and epoxy esters respectively with the peroxide group still intact.

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