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4850-82-2

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4850-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4850-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4850-82:
(6*4)+(5*8)+(4*5)+(3*0)+(2*8)+(1*2)=102
102 % 10 = 2
So 4850-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O4/c1-2-22-18(21)15(16(19)13-9-5-3-6-10-13)17(20)14-11-7-4-8-12-14/h3-12,15H,2H2,1H3

4850-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-benzoyl-3-oxo-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names EINECS 225-442-3

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:4850-82-2 SDS

4850-82-2Relevant articles and documents

2 -amino dibenzo [c, e] azepine compound and synthesis method thereof

-

Paragraph 12-13, (2021/09/15)

The invention belongs to the technical field of organic chemistry, and particularly relates 2 - amine dibenzo [!c, eAzepine compound and a method for synthesizing the same. The method comprises the following steps: in an organic solvent in an inert gas atmosphere and a rare earth catalyst, continuous addition/cyclization reaction of 2 -nitrile -6 - alkynyl biphenyl with an amine to obtain 2 -aminobenzo [!c, eAzepine compound. A core structural unit - of the compound of the present invention is dibenzo [!c, eAzepine is widely found in the synthesis of biologically active molecules and natural products. The synthesis method is novel, has the advantages of mild reaction conditions, easily available raw materials, no need of any additives and additional ligands, no side reaction, high atom economy, simple operation, high product yield and the like.

SmCl3-catalyzed C-acylation of 1,3-dicarbonyl compounds and malononitrile

Shen, Quansheng,Huang, Wen,Wang, Jialiang,Zhou, Xigeng

, p. 4491 - 4494 (2008/03/12)

(Chemical Equation Presented) A recyclable, convenient, and efficient catalytic system for C-acylation of 1,3-dicarbonyl compounds and malononitrile with acid chlorides has been developed, giving moderate to excellent yields under mild conditions. This is the first catalytic example of such reactions. In addition, by applying this protocol as the key step, 3,5-disubstituted-1H- pyrazole-4-carboxylate can easily be synthesized in high yields in a one-pot procedure.

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