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36721-61-6

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36721-61-6 Usage

General Description

The chemical "1-methyl-2-oxo-1,2-dihydr..." (the full chemical name was not provided) likely refers to a ketone compound with a methyl group attached to the second carbon atom. The presence of "2-oxo" in the name suggests that it contains a carbonyl group, which is a carbon atom double-bonded to an oxygen atom. The "1,2-dihydr..." portion of the name indicates that there are two hydrogen atoms attached to the first and second carbon atoms, forming a dihydric structure. 1-methyl-2-oxo-1,2-dihydr... may have various potential uses in organic synthesis, pharmaceuticals, or other chemical applications due to its specific molecular structure.

Check Digit Verification of cas no

The CAS Registry Mumber 36721-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,2 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36721-61:
(7*3)+(6*6)+(5*7)+(4*2)+(3*1)+(2*6)+(1*1)=116
116 % 10 = 6
So 36721-61-6 is a valid CAS Registry Number.

36721-61-6SDS

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-2-oxo-1,2-dihydropyridine-3-methanol

1.2 Other means of identification

Product number -
Other names 3-(hydroxymethyl)-1-methylpyridin-2-one

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:36721-61-6 SDS

36721-61-6Relevant articles and documents

Tether-enforced reversal of regioselectivity: Head-to-head [4 + 4] photocycloaddition of 2-pyridones

Sieburth, Scott McN.,Siegel, Brian

, p. 2249 - 2250 (1996)

Symmetric 3,3′-attachment of a three-atom chain between two pyridones overrides the head-to-tail regioselectivity found in intermolecular photodimerization reactions and gives a nearly quantitative yield of the head-to-head [4 + 4] cycloadduct containing contiguous quaternary centres.

HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF SUMO ACTIVATING ENZYME

-

Paragraph 00191, (2015/01/16)

Disclosed are compounds of formula (I): or a pharmaceutically acceptable salt thereof; wherein Y, Ra, Ra', Rc, Rf, X2, Rd, Rd', Re, Re', m, and G have the values described herein and stereochemical configurations depicted at asterisked positions indicate absolute stereochemistry, useful as inhibitors of Sumo Activating Enzyme (SAE). Further provided are pharmaceutical compositions comprising a compound of the disclosure and methods of using the compositions in the treatment of proliferative, inflammatory, cardiovascular and neurodegenerative diseases or disorders.

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