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3H-Cyclohept[c]isoxazol-3-one,3a,4,5,6,7,8-hexahydro-(8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29068-42-6

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29068-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29068-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,6 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29068-42:
(7*2)+(6*9)+(5*0)+(4*6)+(3*8)+(2*4)+(1*2)=126
126 % 10 = 6
So 29068-42-6 is a valid CAS Registry Number.

29068-42-6SDS

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 1,4,5,6,7,8-hexahydro-cyclohepta[c]isoxazol-3-one

1.2 Other means of identification

Product number -
Other names -

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:29068-42-6 SDS

29068-42-6Downstream Products

29068-42-6Relevant academic research and scientific papers

Atom-Economic Silver-Catalyzed Difunctionalization of the Isocyano Group with Cyclic Oximes: Towards Pyrimidinediones

Liang, Hong-Wen,Yang, Zhen,Jiang, Kun,Ye, Ying,Wei, Ye

supporting information, p. 5720 - 5724 (2018/04/25)

An unprecedented silver-catalyzed difunctionalization of the isocyano group with cyclic oximes is described. This method allows efficient and atom-economic assembly of a vast array of structurally novel and interesting pyrimidinediones, and tolerates a range of functionalities. The resulting products can be easily converted into some useful compounds. Furthermore, the method can also be applied for the late-stage modification of a few biologically active molecules.

Rhodium- and non-metal-catalyzed approaches for the conversion of isoxazol-5-ones to 2,3-dihydro-6H-1,3-oxazin-6-ones

Jurberg, Igor D.,Davies, Huw M.L.

supporting information, p. 5158 - 5161 (2017/11/06)

Two approaches were developed for the conversion of isoxazol-5-ones to 2,3-dihydro-6H-1,3-oxazin-6-ones. The first involves dirhodium-catalyzed reaction of aryl diazoacetates, leading to rhodium carbene intermediates that undergo insertion into the N-O bo

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