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(R)-3-hydroxy-1-methyl-2,5-pyrrolidinedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131237-81-5

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131237-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131237-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,3 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131237-81:
(8*1)+(7*3)+(6*1)+(5*2)+(4*3)+(3*7)+(2*8)+(1*1)=95
95 % 10 = 5
So 131237-81-5 is a valid CAS Registry Number.

131237-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-N-methylsuccinimide

1.2 Other means of identification

Product number -
Other names .3-hydroxy-1-methylpyrrolidin-2,5-dione

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:131237-81-5 SDS

131237-81-5Relevant academic research and scientific papers

Preparation method of 1-methyl-3-pyrrolidinol

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Paragraph 0051; 0056-0058; 0064; 0069-0071; 0077; 0082;..., (2021/09/01)

The invention relates to the technical field of synthesis of medical intermediates, and particularly discloses a preparation method of 1-methyl-3-pyrrolidinol. The preparation method comprises the following steps that S1, a compound I and a compound II are subjected to a ring closing reaction, so a compound III is obtained; and S2, the compound III obtained in the step S1 and a reducing agent IV are subjected to a reduction reaction, so 1-methyl-3-pyrrolidinol is obtained, wherein the compound I, the compound II and the compound III are as shown in the specification; and the reducing agent IV is one or more selected from a group consisting of sodium borohydride, potassium borohydride, boron trifluoride-diethyl ether and boron tribromide-diethyl ether. According to the preparation method, the compound II and the compound I are selected and subjected to the ring closing reaction to obtain the intermediate compound III, and the compound III is solid and is easy to crystallize and purify, so the purification difficulty of the intermediate is reduced, the purity of the intermediate is favorably improved, and the product quality of the 1-methyl-3-pyrrolidinol is further improved.

SYNTHESIS OF AN ANTIVIRAL COMPOUND

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Paragraph 0180; 0181, (2014/03/22)

The present disclosure provides processes for the preparation of a compound of Formula I: which is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of formula.

SYNTHESIS OF AN ANTIVIRAL COMPOUND

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Paragraph 0137, (2014/03/22)

The present disclosure provides a processes for the preparation of a compound of Formula I: which is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of Formula I.

Isothiazolecarboxylic acid derivatives and their use as microbicides

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, (2008/06/13)

Novel isothiazolecarboxylic acid derivatives of the formula (I), in which A, Q, Z and k have the meanings mentioned in the specification, processes for the preparation of the new compounds and their use as microbicides.

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