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42599-26-8

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42599-26-8 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 50, p. 3573, 1985 DOI: 10.1021/jo00219a025

Check Digit Verification of cas no

The CAS Registry Mumber 42599-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42599-26:
(7*4)+(6*2)+(5*5)+(4*9)+(3*9)+(2*2)+(1*6)=138
138 % 10 = 8
So 42599-26-8 is a valid CAS Registry Number.

42599-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-oxo-2-pyrrolidone

1.2 Other means of identification

Product number -
Other names 1-methyl-2,3-pyrrolidindion

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:42599-26-8 SDS

42599-26-8Relevant articles and documents

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Bender et al.

, p. 1264,1266, 1268 (1975)

-

SMALL MOLECULE INHIBITORS OF NF-kB INDUCING KINASE

-

Page/Page column 129, (2020/12/11)

The present invention relates to compounds that inhibit NIK and pharmaceutical compositions comprising such compounds and methods of using the same. These compounds and pharmaceutical compositions are envisaged to be useful for preventing or treating diseases such as cancer (such as B-cell malignancies including leukemias, lymphomas and myeloma), inflammatory disorders, autoimmune disorders, immunodermatologic disorders such as palmoplantar pustulosis and hidradenitis suppurativa, and metabolic disorders such as obesity and diabetes.

Reaction of Singlet Oxygen with Enamino Carbonyl Systems. A General Method for the Synthesis of α-Keto Derivatives of Lactones, Esters, Amides, Lactams, and Ketones

Wasserman, Harry H.,Ives, Jeffrey L.

, p. 3573 - 3580 (2007/10/02)

A general method for the introduction of a ketone α to the carbonyl group of a ketone, lactone. ester, substituted amide, or lactam has been developed involving the formation and dye-sensitized photooxygenation of enamino carbonyl intermediates.

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