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2-oxodecanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16979-02-5

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16979-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16979-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16979-02:
(7*1)+(6*6)+(5*9)+(4*7)+(3*9)+(2*0)+(1*2)=145
145 % 10 = 5
So 16979-02-5 is a valid CAS Registry Number.

16979-02-5SDS

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 2-oxodecanal

1.2 Other means of identification

Product number -
Other names 2-oxo-decanal

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:16979-02-5 SDS

16979-02-5Downstream Products

16979-02-5Relevant articles and documents

PHOSPHOLIPASE A2 INHIBITORS

-

, (2008/06/13)

There are disclosed compounds of the formula: wherein R1 is hydrogen, alkyl, cycloalkyl, arylalkyl, -(CH2)rCH=CH2, -(CH2)sOY, -(CH2)tCH(OZ)CH3, or Ar; X is O, S, or NR2; Y and Z are each, independently, hydrogen, alkyl, or ?COR3; R2 and R3 are each, independently, hydrogen, alkyl, or arylalkyl; Ar is an aryl radical that may be optionally substituted; m=1-5; n=0-1; p=1-9; r=0-6; s=2-6; and t=0-6 or a pharmaceutically acceptable salt thereof which are useful as antiinflammatory agents

Molecular oxygen oxidative carbon-carbon bond cleavage of α-ketols catalysed by Bi(III) carboxylates

Le Boisselier, Veronique,Coin, Christine,Postel, Michele,Dunach, Elisabet

, p. 4991 - 4996 (2007/10/02)

Bi(III)-mandelate catalyses the oxidative carbon-carbon bond cleavage, by molecular oxygen, of a series of α-ketols into the corresponding carboxylic acids. The reaction is accelerated in the presence of DMSO.

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