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2,5-Piperazinedione,3-ethyl-6-(1-methylethyl)-,(3S,6S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

407578-43-2

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407578-43-2 Usage

General Description

2,5-Piperazinedione,3-ethyl-6-(1-methylethyl)-,(3S,6S)-(9CI) is a chemical compound with the molecular formula C10H18N2O2. It is a piperazinedione derivative with a 3-ethyl-6-(1-methylethyl) substituent. The compound exists as a stereoisomer with a 3S,6S configuration. It is commonly used as a reagent in chemical reactions and has potential applications in pharmaceutical research and development. The compound's precise properties and uses may vary depending on the specific application and context in which it is used.

Check Digit Verification of cas no

The CAS Registry Mumber 407578-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,7,5,7 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 407578-43:
(8*4)+(7*0)+(6*7)+(5*5)+(4*7)+(3*8)+(2*4)+(1*3)=162
162 % 10 = 2
So 407578-43-2 is a valid CAS Registry Number.

407578-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,6S)-3-isopropyl-6-ethylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names (3S,6S)-3-ETHYL-6-(1-METHYLETHYL)PIPERAZINE-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:407578-43-2 SDS

407578-43-2Relevant academic research and scientific papers

Conjugate additions of organocuprates to a 3-methylene-6-isopropyldiketopiperazine acceptor for the asymmetric synthesis of homochiral α-amino acids

Bull,Davies,Garner,O'Shea

, p. 3281 - 3287 (2007/10/03)

Addition of a range of organocuprates to (S)-N,N′-bis(p-methoxybenzyl)-3-methylene-6-isopropylpiperazine-2, 5-dione 8 affords cis-3-isopropyl-6-alkyldiketopiperazines in excellent yield and >95% de. Subsequent deprotection and hydrolysis of these cis-3-isopropyl-6-alkyldiketopiperazines affords homochiral (S)-α-amino acids in excellent yield.

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