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4,6-bis(methoxyamino)-5,6-dihydropyrimidin-2(1H)-one is a chemical compound belonging to the pyrimidine family, characterized by a heterocyclic structure with two nitrogen atoms and a double bond between carbon and nitrogen. This specific compound features two methoxyamino groups attached to the 4 and 6 positions of the pyrimidine ring, and a 5,6-dihydro structure, indicating the presence of a double bond between carbons 5 and 6, which is reduced to a single bond, creating a saturated six-membered ring. The compound has a 2(1H)-one functional group, signifying a ketone group at the 2-position with one hydrogen atom attached, which can participate in various chemical reactions. 4,6-bis(methoxyamino)-5,6-dihydropyrimidin-2(1H)-one may have potential applications in pharmaceuticals or as an intermediate in organic synthesis due to its unique structure and reactivity.

3572-87-0

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3572-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3572-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3572-87:
(6*3)+(5*5)+(4*7)+(3*2)+(2*8)+(1*7)=100
100 % 10 = 0
So 3572-87-0 is a valid CAS Registry Number.

3572-87-0SDS

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 4,6-bis(methoxyamino)-5,6-dihydro-1H-pyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 4,5-Dihydro-N6-methoxy-4-methoxyamino-cytosin

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:3572-87-0 SDS

3572-87-0Downstream Products

3572-87-0Relevant academic research and scientific papers

Stereochemistry of the Formation of 4-Alkoxyimino-5,6-dihydro-6-alkoxyaminopyrimidin-2(1H)-ones from Cytosines and Hydroxylamines

Atkins, Paul J.,Hall, C. Dennis

, p. 155 - 160 (2007/10/02)

High resolution 1H and 19F n.m.r. data together with deuterium labelling studies are presented which reveal that the addition of hydroxylamines across the 5,6-double bond of cytosines is predominantly trans.The 4-alkoxyimino-5,6-dihydro-6-alkoxyaminopyrimidin-2(1H)-one products show syn/anti isomerism about the 4-alkoxyimino-group dependent on the substituent at N(3) (H or Me, respectively) and conformational changes throughout the molecules which are dependent on the substituents at N(1) (H or Me) and C(5) (H or F).

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