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22945-27-3

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22945-27-3 Usage

Chemical Properties

off-yellow or white crystallline powder

Check Digit Verification of cas no

The CAS Registry Mumber 22945-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22945-27:
(7*2)+(6*2)+(5*9)+(4*4)+(3*5)+(2*2)+(1*7)=113
113 % 10 = 3
So 22945-27-3 is a valid CAS Registry Number.

22945-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxocyclohexane-1-carboxamide

1.2 Other means of identification

Product number -
Other names 2-oxo-1-cyclohexanecarboxamide

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:22945-27-3 SDS

22945-27-3Relevant articles and documents

Synthesis process of gliclazide intermediate 2-formamide cyclohexanone

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Paragraph 0018-0042, (2021/04/17)

The invention provides a synthesis process of a gliclazide intermediate 2-formamide cyclohexanone, and relates to the technical field of synthesis of gliclazide intermediates. According to the synthesis process disclosed by the invention, after the reaction kettle is cooled in advance, the solvent xylene and the raw material urea are added and the catalyst tetrabutyl titanate is added, the spiro intermediate can be generated through high-selectivity catalysis along with the addition of cyclohexanone, and the reaction condition of high-temperature azeotropy is not needed; ketone can be hydrolyzed and removed only at a low temperature after heating, water adding and stirring are carried out; after xylene and residual cyclohexanone are removed from the filtrate through vacuum concentration, ethanol is used for dispersing the crude product of the 2formamide cyclohexanone, and sodium bicarbonate is used for neutralizing generated hydrogen ions, so that the neutral environment of the system is maintained, and a pure product of the 2-formamide cyclohexanone with high yield and purity is obtained after subsequent filtration and crystallization.

Synthesizing process for improving yield of gliclazide intermediate 2-formamide cyclohexanone

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Paragraph 0020-0021, (2017/01/09)

The invention provides a synthesizing process for improving the yield of a gliclazide intermediate 2-formamide cyclohexanone. According to the invention, on the basis of an original process, a novel catalyst titanium(IV) isopropoxide is added into a reaction system, such that a synthesis yield is improved from 82% to 90% while product quality is improved. The process has significant economic benefits.

Facile carbethoxylation and carbamoylation of ketones

Pazdera, Pavel,Simbera, Jan

experimental part, p. 297 - 301 (2011/08/06)

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