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3,4-Piperidinediol, 1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61862-67-7

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61862-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61862-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,6 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61862-67:
(7*6)+(6*1)+(5*8)+(4*6)+(3*2)+(2*6)+(1*7)=137
137 % 10 = 7
So 61862-67-7 is a valid CAS Registry Number.

61862-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylpiperidine-3,4-diol

1.2 Other means of identification

Product number -
Other names 1-Methyl-piperidin-3,4-diol

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:61862-67-7 SDS

61862-67-7Downstream Products

61862-67-7Relevant academic research and scientific papers

Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks

Dupau, Philippe,Epple, Robert,Thomas, Allen A.,Fokin, Valery V.,Sharpless, K. Barry

, p. 421 - 433 (2007/10/03)

A screen of over 500 diversely functionalized additives in osmium-catalyzed dihydroxylation has uncovered that electron-deficient olefins are converted into the corresponding diols much more efficiently when the pH of the reaction medium is maintained on the acidic side. Further studies have identified citric acid as the additive of choice, for it allows preparation of very pure diols in yields generally exceeding 90%. As described here, a much wider range of olefin classes can now be successfully dihydroxylated. The process is experimentally simple, in most cases involving little more than dissolving the reactants in water or a waler/tertbutyl alcohol mixture, stirring them, and filtering off the pure diol product.

Cephalosporin compounds and processes for preparing thereof

-

, (2008/06/13)

Quaternary ammoniocephalosporins of formula(I) wherein Q=CH or N, P=hydroxylated amine or hydroxylated heterocyclylamines including N-methyl-bis(2-hydroxyethyl)amine, rac-3,4-trans-dihydroxy-1-methylpyrrolidine, (3S, 4S)-3,4-dihydroxy-1-methylpyrrolidine,

STUDY OF THE HYDROXYLATION OF N-SUBSTITUTED 1,2,5,6-TETRAHYDROPYRIDINES

Maksimova, T. N.,Mochalin, V. B.,Unkovskii, B. V.

, p. 604 - 607 (2007/10/02)

N-Substituted 1,2,5,6-tetrahydropyridines are readily converted to the corresponding 1,2-diols by treatment with an aqueous solution of potassium permanganate in a neutral medium.The yields of the desired products depend on the character of the substituent attached to the nitrogen atom and decrease in the case of N-methyl-1,2,5,6-tetrahydropyridines as a consequence of the formation of side products formed as a result of more profound oxidation.The acylation of the synthesized diols was studied.The three-dimensional structures of the synthesized cis-diols were established by IR spectroscopy.

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