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19780-10-0

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19780-10-0 Usage

Synthesis Reference(s)

Synthesis, p. 89, 1990Tetrahedron Letters, 26, p. 3595, 1985 DOI: 10.1016/S0040-4039(00)89199-6

Check Digit Verification of cas no

The CAS Registry Mumber 19780-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19780-10:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*1)+(1*0)=130
130 % 10 = 0
So 19780-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O/c1-3-5-7-8-9-11-12(13)10-6-4-2/h3-11H2,1-2H3

19780-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecan-5-one

1.2 Other means of identification

Product number -
Other names Dodecan-5-on

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:19780-10-0 SDS

19780-10-0Downstream Products

19780-10-0Relevant articles and documents

SELENOESTERS IN ORGANIC SYNTHESIS. 2. NEW SYNTHESIS OF SATURATED AND α,β-UNSATURATED KETONES AND THE SYNTHESIS OF THE PEACH MOTH PHEROMONE (Carposia niponensis)

Sviridov, A. F.,Ermolenko, M. S.,Yashunskii, D. V.,Kochetkov, N. K.

, p. 1514 - 1518 (1985)

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Selective Ketone Formations via Cobalt-Catalyzed β-Alkylation of Secondary Alcohols with Primary Alcohols

Pandey, Bedraj,Xu, Shi,Ding, Keying

supporting information, p. 7420 - 7423 (2019/10/02)

A homogeneous cobalt-catalyzed β-alkylation of secondary alcohols with primary alcohols to selectively synthesize ketones via acceptorless dehydrogenative coupling is reported for the first time. Notably, this transformation is environmentally benign and atom economical with water and hydrogen gas as the only byproducts.

Simple one pot synthesis of ketone from carboxylic acid using DCC as an activator

Mekonnen, Habtamu Gelaw,Jana, Samaresh

supporting information, p. 1382 - 1384 (2019/04/30)

Simple one pot procedure for the conversion of carboxylic acid to ketone is described. Various carboxylic acids were converted to the corresponding ketones in excellent manner in presence of N,N′-dicyclohexylcarbodiimide (DCC) and organometallic reagents. Aromatic, heteroaromatic and aliphatic acids were converted to the corresponding ketones smoothly under the optimum conditions using organolithium reagents. In this process, desired products have been isolated from the crude reaction mixtures in moderate yields during the purification process.

Nickel-catalyzed cross-coupling of non-activated and functionalized alkyl halides with alkyl grignard reagents

Vechorkin, Oleg,Hu, Xile

supporting information; experimental part, p. 2937 - 2940 (2009/09/08)

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