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155225-26-6

155225-26-6

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155225-26-6 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 155225-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,2 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155225-26:
(8*1)+(7*5)+(6*5)+(5*2)+(4*2)+(3*5)+(2*2)+(1*6)=116
116 % 10 = 6
So 155225-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O3/c1-3-5(10)8-4(2-9)6(11)7-3/h3-4,9H,2H2,1H3,(H,7,11)(H,8,10)/t3-,4-/m0/s1

155225-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,6S)-3-(hydroxymethyl)-6-methylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names (S)-3-hydroxymethyl-1-methylpiperazine-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:155225-26-6 SDS

155225-26-6Upstream product

155225-26-6Relevant articles and documents

The synthetic versatility of alkoxycarbonyl- and hydroxymethyl-piperazine- 2,5-diones

Chai, Christina L.L.,Elix, John A.,Huleatt, Paul B.

, p. 8722 - 8739 (2007/10/03)

Alkoxycarbonylpiperazine-2,5-diones are versatile precursors for the α-functionalisation of piperazine-2,5-diones. The alkoxycarbonyl group activates the α-carbon position to alkylation reactions and this provides a mild and selective method for the extension of the carbon framework of piperazine-2,5-diones. In addition, the alkoxycarbonyl group can be converted to the carboxy group, which in turn can be 'deleted' or manipulated for the installation of carbon and/or heteroatom substituents where desired, the latter via N-acyliminium chemistry. We also demonstrate that hydroxymethylpiperazine-2, 5-diones complement carboxypiperazinediones as precursors for the generation of N-acyliminium ions.

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