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10166-54-8

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10166-54-8 Usage

Uses

1-Methyltetrahydro-2(1H)-pyrimidinone is a thiourea derivative used as nducers of murine erythroleukemia differentiation.

Check Digit Verification of cas no

The CAS Registry Mumber 10166-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,6 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10166-54:
(7*1)+(6*0)+(5*1)+(4*6)+(3*6)+(2*5)+(1*4)=68
68 % 10 = 8
So 10166-54-8 is a valid CAS Registry Number.

10166-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyltetrahydropyrimidin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 1-methyl-1,3-diazinan-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:10166-54-8 SDS

10166-54-8Relevant articles and documents

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Fox,van Praag

, p. 486,488 (1960)

-

Catalytic oxidative carbonylation of primary and secondary α,ω-diamines to cyclic ureas

McCusker, Jennifer E.,Grasso, Cara A.,Main, Andrea D.,McEiwee-White, Lisa

, p. 961 - 964 (1999)

(matrix presented) Primary and secondary diamines can be catalytically carbonylated to cyclic ureas using W(CO)6 as the catalyst, I2 as the oxidant, and CO as the carbonyl source. Preparation of five-, six-, and seven-membered cyclic ureas from the diamines RNHCH2(CH2)nCH2NHR (n = 0-2; R = H, Me) and RNHCH2CH2NHR (R = Et, i-Pr, Bz) was achieved in moderate to good yields.

PROCESS FOR THE PRODUCTION OF CYCLIC GUANIDINE DERIVATES

-

Page/Page column 10-11, (2021/04/30)

The present invention relates to a process for the production of cyclic guanidine derivates of formula I or mixtures of them (formula I) by reacting a triamine in the present of a C1-source and a solid material in the gas or liquid phase under inert atmosphere.

3-(Triflyloxy)benzynes Enable the Regiocontrolled Cycloaddition of Cyclic Ureas to Synthesize 1,4-Benzodiazepine Derivatives

Kaneko, Hideki,Ikawa, Takashi,Yamamoto, Yuta,Arulmozhiraja, Sundaram,Tokiwa, Hiroaki,Akai, Shuji

supporting information, p. 943 - 948 (2018/02/26)

A versatile synthesis of 1,4-benzodiazepine derivatives through the reaction of various 3-(trifluoromethanesulfonyloxy)benzynes with N -(p -toluenesulfonyl)imidazolidin-2-ones is reported. This reaction system provides a 1,4-benzodiazepine bearing a trifluoromethanesulfonyloxy group as a single regioisomer among the four possible regioisomers.

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