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23055-10-9

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23055-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23055-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23055-10:
(7*2)+(6*3)+(5*0)+(4*5)+(3*5)+(2*1)+(1*0)=69
69 % 10 = 9
So 23055-10-9 is a valid CAS Registry Number.

23055-10-9SDS

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 dimethyl (2E)-but-2-enedioate (en)2-Butenedioic acid, dimethyl ester (en)

1.2 Other means of identification

Product number -
Other names Phosphoric acid,dimethyl ethyl ester

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:23055-10-9 SDS

23055-10-9Relevant articles and documents

Vinyltriphenylphosphonium salt mediated synthesis of 1,4-benzoxazine and coumarin derivatives

Yavari, Issa,Adib, Mehdi,Hojabri, Leila

, p. 6895 - 6899 (2002)

Protonation of the reactive 1:1 intermediate produced in the reaction between triphenylphosphine and dimethyl acetylenedicarboxylate by 2-aminophenol, 3-aminophenol, 4-aminophenol and 2-amino-3-hydroxypyridine leads to vinyltriphenylphosphonium salts, whi

Microwave-specific acceleration of a retro-Diels-Alder reaction

Dudley, Gregory B.,Frasso, Michael A.,Stiegman, Albert E.

supporting information, p. 11247 - 11250 (2020/10/06)

A high-temperature retro-Diels-Alder reaction is accelerated by microwave (MW) heating to rates higher than expected based on Arrhenius kinetics and the measured temperature of the reaction mixture. Observations are consistent with selective MW heating of the polar reactant relative to other, less polar components of the reaction mixture.

Three-component reaction of triphenylphosphine, dialkyl acetylenedicarboxylates, and heterocyclic rings and the related iminophosphoranes

Anary-Abbasinejad, Mohammad,Hassanabadi, Alireza,Khaksari, Zahra

, p. 204 - 212 (2011/10/31)

Crystalline phosphorus ylides are obtained in excellent yields from the 1:1:1 addition reaction of triphenylphosphine, dialkyl acetylenedicarboxylate, and NH acids, such as 2-aminothiazole and 2-aminobenzothiazole. These stabilized phosphoranes undergo a

Effect of imidazolium salts on the catalytic reaction of 1,3-dioxolanes with methyl diazoacetate

Ivanova,Sultanova,Zlotskii

experimental part, p. 106 - 108 (2011/06/18)

Effect of imidazolium salts, [bmim]+Cl-, [bmim] +BF4 -, and [bmim]+PF6 -, on the reaction of 1,3-dioxolanes with methyl diazoacetate in the presence of copper-containing catalysts was studied. The product composition was found to depend on the reaction conditions and the nature and ratio of components of the catalytic system.

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