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2,4-Cyclohexadiene-1,2-dicarboxylic acid, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90295-61-7

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90295-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90295-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,9 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90295-61:
(7*9)+(6*0)+(5*2)+(4*9)+(3*5)+(2*6)+(1*1)=137
137 % 10 = 7
So 90295-61-7 is a valid CAS Registry Number.

90295-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl cyclohexa-2,4-diene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names Cyclohexa-1,3-dien-1,6-dicarbonsaeure-dimethylester

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:90295-61-7 SDS

90295-61-7Downstream Products

90295-61-7Relevant academic research and scientific papers

Synthesis of novel fluorinated building blocks via halofluorination and related reactions

Fül?p, Ferenc,Haukka, Matti,Kiss, Loránd,Nonn, Melinda,Novák, Tamás T.,Remete, Attila Márió

supporting information, p. 2562 - 2575 (2020/11/20)

A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions of the ring olefin bonds, followed by nucleophilic fluorination with Deoxo-Fluor. The fluorine-containing products thus obtained were subjected to elimination reactions, yielding various fluorine-containing small-molecular entities.

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